Internalizing human monoclonal antibodies targeting prostate cancer cells in situ

ABSTRACT

This invention provides a method that allows selection of antibodies against cells (e.g., tumor cells) in situ using laser capture microdissection. By restricting antibody selection to binders of internalizing epitopes, a panel of phage antibodies was generated that targets clinically represented prostate cancer antigens.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. Ser. No. 16/596,684, filed onOct. 8, 2019, which is a divisional of U.S. Ser. No. 15/418,588, filedon Jan. 27, 2017, issued as U.S. Pat. No. 10,479,839, which is adivisional of U.S. Ser. No. 14/486,943, filed on Sep. 15, 2014, issuedas U.S. Pat. No. 9,593,162, which is a divisional of U.S. Ser. No.12/724,282, filed on Mar. 15, 2010, issued as U.S. Pat. No. 8,865,873,which is a continuation-in-part of PCT/US2008/076704 (WO/2009/039192),filed on Sep. 17, 2008, which claims benefit of and priority to U.S.Ser. No. 60/973,005, filed on Sep. 17, 2007, all of which areincorporated herein by reference in their entirety for all purposes.

STATEMENT AS TO RIGHTS TO INVENTIONS MADE UNDER FEDERALLY SPONSOREDRESEARCH AND DEVELOPMENT

This invention was made with government support under grant nos. RO1CA118919, DK066428 and P50 CA089520 awarded by The National Institutesof Health. The government has certain rights in the invention.

INCORPORATION BY REFERENCE OF SEQUENCE LISTING PROVIDED AS AN XML FILE

This application contains references to nucleic acid sequences that havebeen submitted concurrently herewith as the sequence listing ST26 formatXML file “UCSFP028X1D3C1.xml”, file size 448,525 bytes, created on Oct.4, 2023, which is incorporated by reference in its entirety pursuant to37 C.F.R. § 1.52(e)(5).

FIELD OF THE INVENTION

This invention pertains to the field of antibodies, immunodiagnostics,and immunotherapeutics. In particular, this invention pertains to novelmethods for in vivo screening of antibodies and the discovery ofprostate cancer specific internalizing antibodies using such methods.

BACKGROUND OF THE INVENTION

Due to ease of accessibility, tumor cell surface antigens are invaluabletargets for therapeutic development. The epitope space at the cellsurface is highly complex. Relevant antigens may include glycosylatedproteins and other post-translationally modified products that may notbe readily predicted from studies of genomic copy number or mRNAexpression levels (Liu et al. (2004) Cancer Res. 64: 704-710; Kobata andAmano (2005) Immunol. Cell Biol. 83: 429-439; Birkle et al. (2003)Biochimie (Paris) 85: 455-463; Hakomori (2001) Adv. Exp. Med. Biol. 491:369-402; Hanisch, F. G. (2001) 0-Glycosylation of the mucin type. Biol.Chem. 382, 143-149; Ugorski and Laskowska (2002)Acta Biochim. Pol. 49:303-311).

Because monoclonal antibodies (mAbs) recognize a wide range of antigenicdeterminants with high affinity and specificity and are able to discernsubtle differences in antigen structure and conformation, they can beused to efficiently map the tumor cell surface epitope space (Liu et al.(2004) Cancer Res. 64, 704-710). Isolating these epitopes enables theantibodies to achieve specific binding to neoplastic cells, an abilitythat could be utilized in applications such as induction ofantibody-dependent cell cytotoxicity (Clynes et al. (2000) Nat. Med. 6:443-446) or inhibition of signaling pathways involved in tumor cellmigration, growth, and survival (McWhirter et al. (2006) Proc. Natl.Acad. Sci., USA, 103: 1041-1046; Fuh et al. (2006) J. Biol. Chem. 281:6625-6631). In addition, antibodies targeting internalizing tumorepitopes could be exploited to achieve efficient and specificintracellular delivery of chemotherapeutic drugs and/or othertumor-modulating agents (Liu et al. (2004) Cancer Res. 64: 704-710;Nielsen et al. (2002) Biochim. Biophys. Acta 1591: 109-118; Pirollo etal. (2006) Hum. Gene Ther. 17: 117-124; Song et al. (2005) Nat.Biotechnol. 23:709-717; Liu et al. (2002) J Mol. Biol. 315: 1063-1073).

Phage antibody display has been widely used to develop cancer-specificantibodies (Liu et al. (2004) Cancer Res. 64: 704-710; Liu and Marks(2000) Anal. Biochem. 286: 119-128; 15. Marks et al. (1992)Biotechnology (N. Y.) 10: 779-783; Marks et al. (1991) J Mol. Biol. 222:581-597; Marks et al. (1992) J Biol. Chem. 267: 16007-16010; Sharon etal. (2005) J Cell. Biochem. 96: 305-313; Silacci et al. (2005)Proteomics 5: 2340-2350; Gao et al. (2003) J Immunol. Methods 274:185-197; Lekkerkerker and Logtenberg (1999) J Immunol. Meth., 231:53-63; de Kruif et al. (1995) Proc. Natl. Acad. Sci., USA, 92:3938-3942; Pini et al. (1998) J Biol. Chem. 273: 21 769-21 776). Acombinatorial phage antibody library serves as a source of random shaperepertoire that can be used to probe neoplastic variations on thesurface of cancer cells (Liu et al. (2004) Cancer Res. 64: 704-710;Geuijen et al. (2005) Eur. J. Cancer 41: 178-187; Poul et al. (2000) J.Mol. Biol. 301: 1149-1161; Cai and Garen (1995) Proc. Natl. Acad. Sci.,USA, 92: 6537-6541). Selecting phage antibody libraries directly oncancer cell lines enables the identification of tumor-targetingantibodies without prior knowledge of target antigens (Liu et al. (2004)Cancer Res. 64: 704-710; Gao et al. (2003) J. Immunol. Methods 274:185-197; Geuijen et al. (2005) Eur. J. Cancer 41: 178-187; Poul et al.(2000) J. Mol. Biol. 301: 1149-1161). Although numerous antibodies havebeen found by this approach, the screening process against cell linesdoes not provide an ideal picture as to how specific these antibodieswill be to actual cancer cells in patient populations. After severalgenerations in culture, cancer cell lines may express cell surfaceepitopes that differ from those present in the original canceroustissue. Tissue sections from cancer patients would be an ideal selectiontarget in the development of cancer-specific antibodies; however, mosttissues taken during surgeries, biopsies, or autopsies are composed ofheterogeneous cell populations. This seemingly poses a serious obstacleto selection methods that would specifically target cancer cells intissue.

SUMMARY OF THE INVENTION

In certain embodiments this invention pertains to the development of amethod that allows selection of antibodies against tumor cells in situusing laser capture microdissection. By restricting antibody selectionto binders of internalizing epitopes, a panel of phage antibodies thattarget clinically represented prostate cancer antigens was generated.

Accordingly, in certain embodiments this invention provides an isolatedantibody that specifically binds and, optionally, is internalized into aprostate cancer cell. In various embodiments the antibody is an antibodythat specifically binds to an epitope that is specifically bound bybound an antibody selected from the group consisting of e.g., 3051.1,G12FC3, M6c42b, 4F3YW, M40pr146, UA20, UA8, 585II41, 585II41.1, 585II56,3076, 3051, M49R, RCI-14, I179_4, I179_3, T5II-4B.1, T5II-4B.2, RCI-11,RCI-20, CI-11A, CI-14A, and/or S95-2. In various embodiments theantibody comprises one, two, or three complementarity determiningregions (CDRs of the variable light (VL domain of an antibody selectedfrom the group consisting of e.g., 3051.1, G12FC3, M6c42b, 4F3YW,M40pr146, UA20, UA8, 585II41, 585II41.1, 585II56, 3076, 3051, M49R,RCI-14, I179_4, I179_3, T5II-4B.1, T5II-4B.2, RCI-11, RCI-20, CI-11A,CI-14A, and/or S95-2; and/or one, two, or three complementaritydetermining regions (CDRs of the variable heavy (VH domain of anantibody selected from the group consisting of e.g., 3051.1, G12FC3,M6c42b, 4F3YW, M40pr146, UA20, UA8, 585II41, 585II41.1, 585II56, 3076,3051, M49R, RCI-14, 1179_4, 11793, T5II-4B.1, T5II-4B.2, RCI-11, RCI-20,CI-11A, CI-14A, and/or S95-2. In certain embodiments the antibodycomprises the three VH CDRs and/or the three VL CDRs of an antibodyselected from the group consisting of e.g., 3051.1, G12FC3, M6c42b,4F3YW, M40pr146, UA20, UA8, 585II41, 585II41.1, 585II56, 3076, 3051,M49R, RCI-14, II79_4, I179_3, T5II-4B.1, T5II-4B.2, RCI-11, RCI-20,CI-11A, CI-14A, and/or S95-2. In certain embodiments the antibodycomprises the VH domain and/or the VL domain of an antibody selectedfrom the group consisting of e.g., 3051.1, G12FC3, M6c42b, 4F3YW,M40pr146, UA20, UA8, 585II41, 585II41.1, 585II56, 3076, 3051, M49R,RCI-14, I179_4, I179_3, T5II-4B.1, T5II-4B.2, RCI-11, RCI-20, CI-11A,CI-14A, and/or S95-2. In various embodiments the antibody is a singlechain antibody. In certain embodiments the VL region is attached to theVH region by a (Gly₄Ser₃ SEQ ID NO:(SEQ ID NO:1) linker. In certainembodiments the antibody is an intact full antibody, a Fab, an (Fab′)₂,an scFv, and an (ScFv′0₂, a unibody, or an affibody. In certainembodiments the antibody comprises a diabody. In certain embodiments theantibody is a single chain antibody selected from the group consistingof 3051.1, G12FC3, M6c42b, 4F3YW, M40pr146, UA20, UA8, 585II41,585II41.1, 585II56, 3076, 3051, M49R, RCI-14, I179_4, I179_3, T5II-4B.1,T5II-4B.2, RCI-11, RCI-20, CI-11A, CI-14A, and S95-2.

In various embodiments chimeric moieties are provided comprising aneffector attached to any one or more of the antibodies described herein.In certain embodiments the effector is selected from the groupconsisting of an epitope tag, a second antibody, a label, a cytotoxin, aliposome, a radionuclide, a drug, a prodrug, a viral particle, acytokine, and a chelate. In certain embodiments the effector comprisesan epitope tag selected from the group consisting of an avidin, and abiotin. In certain embodiments the effector comprises a cytotoxinselected from the group consisting of a Diphtheria toxin, a Pseudomonasexotoxin, a ricin, an abrin, and a thymidine kinase. In certainembodiments the effector comprises a chelate comprising a metal isotopeselected from the group consisting of ⁹⁹Tc, ²⁰³Pb, ⁶⁷Ga, ⁶⁸Ga, ⁷²As,¹¹¹In, ¹¹³In, ⁹⁷Ru, ⁶²Cu, ⁶⁴¹Cu, ⁵²Fe, ⁵²Mn, ⁵¹Cr, ¹⁸⁶Re, ¹⁸⁸Re, ⁷⁷As,⁹⁰Y, ⁶⁷Cu, ¹⁶⁹Er, ¹²¹Sn, ¹²⁷Te, ¹⁴²Pr, ¹⁴³Pr, ¹⁹⁸Au, ¹⁹⁹Au, ¹⁶¹Tb,¹⁰⁹Pd, ¹⁶⁵Dy, ¹⁴⁹Pm, ¹⁵¹Pm, ¹⁵³Sm, ¹⁵⁷Gd, ¹⁵⁹Gd, ¹⁶⁶Ho, ¹⁷²Tm, ¹⁶⁹Yb,¹⁷⁵Yb, ¹⁷⁷Lu, ¹⁰⁵Rh, and ¹¹¹Ag. In certain embodiments the effectorcomprises an alpha emitter (e.g., bismuth 213). In certain embodimentsthe effector is a chelate comprising DOTA. In certain embodiments theeffector comprises a lipid or a liposome.

Also provided are pharmaceutical formulations comprising apharmaceutically acceptable excipient and an antibody or a chimericmoiety as described herein. In certain embodiments the pharmaceuticalformulation of claim is a unit dosage formulation. In certainembodiments the pharmaceutical formulation is formulated foradministration by a route such as intraperitoneal administration,intravenous injection, intramuscular injection, subcutaneousadministration, direct administration to a tumor and/or surgical site,transcutaneous administration, subcutaneous depot formulation, oraladministration, inhalation administration, rectal administration and thelike.

In various embodiments methods are provided for delivering an effectorto a prostate cancer cell. The methods typically involve administeringto a cell, tissue, or organism, a composition comprising an antibody asdescribed herein attached to an effector; whereby the antibodypreferentially interacts with a prostate cancer cell thereby deliveringthe effector to the prostate cancer cell. In certain embodiments thepreferentially interacting comprises being internalized by said cancercell. In certain embodiments the effector comprises an anti-cancer agentand/or a detectable label. In certain embodiments the administeringcomprises administering to a human or to a non-human mammal. In certainembodiments the administering comprises administering parenterally. Incertain embodiments the administering comprises administering into atumor or a surgical site.

In various embodiments methods are provided for inhibiting the growth orproliferation of a prostate cancer cell. The methods typically involvecontacting the cancer cell with an antibody as described herein and/orwith a chimeric moiety comprising one or more antibodies as describedherein attached to an anti-cancer drug (e.g., a lipid complexed with ananti-cancer drug, a liposome containing an anti-cancer drug, etc.), or aradionuclide. In certain embodiments the cancer cell is a metastaticcell. In certain embodiments the cancer cell is a solid tumor cell.

In certain embodiments methods are also provided for detecting aprostate cancer cell. The methods typically involve contacting theprostate cancer cell with a chimeric molecule comprising an antibody asdescribed herein attached to a detectable label; and detecting thepresence and/or location of said detectable label where the presenceand/or location is an indicator of the location and/or presence of aprostate cancer cell. In certain embodiments the detectable label isselected from the group consisting of a gamma-emitter, apositron-emitter, an x-ray emitter, an alpha emitter, and afluorescence-emitter. In certain embodiments the methods typicallyinvolve contacting a prostate cancer cell with a chimeric moleculecomprising an antibody as described herein attached to an epitope tag;contacting the chimeric molecule with a chelate comprising a detectablemoiety whereby the chelate binds to the epitope tag thereby associatingsaid detectable moiety with the chelate; and detecting the detectablemoiety where the presence and/or location of the detectable moiety is anindicator of the location and/or presence of a prostate cancer cell. Incertain embodiments the detectable moiety or detectable label is aradionuclide. In certain embodiments the detectable moiety or detectablelabel is selected from the group consisting of a gamma-emitter, apositron-emitter, an alpha emitter, an x-ray emitter, and afluorescence-emitter. In certain embodiments the detecting comprisesexternal imaging. In certain embodiments the detecting comprisesinternal imaging. In certain embodiments the detectable moiety ordetectable label comprises a metal isotope selected from the groupconsisting of to ⁹⁹Tc, ²⁰³Pb, ⁶⁷Ga, ⁶⁸Ga, ⁷²As, ¹¹¹In, ^(113m)In, ⁹⁷Ru,⁶²Cu, ⁶⁴¹Cu, ⁵²Fe, ^(52m)Mn, ⁵¹Cr, ¹⁸⁶, Re, ¹⁸⁸Re, ⁷⁷As, ⁹⁰Y, ⁶⁷Cu,¹⁶⁹Er, ¹²¹Sn, ¹²⁷Te, ¹⁴²Pr, ¹⁴³Pr, ¹⁹⁸Au, ¹⁹⁹Au, ¹⁶¹Tb, ¹⁰⁹Pd, ¹⁶⁵Dy,¹⁴⁹Pm, ¹⁵¹Pm, ¹⁵³Sm, ¹⁵⁷Gd, ¹⁵⁹Gd, ¹⁶⁶Ho, ¹⁷²Tm, ¹⁶⁹Yb, ¹⁷⁵Yb, ¹⁷Lu,^(99m)Tc, ¹⁰⁵Rh, and ¹¹¹Ag. In certain embodiments the chelate comprisesDOTA. In certain embodiments the epitope tag is an avidin or a biotin.

Also provided are nucleic acids encoding an antibody as describedherein. In various embodiments the nucleic acids comprise a vector andcan be present in a cell whereby the cell expresses the antibody.

In various embodiments, this invention provides methods of identifyingan antibody that preferentially binds to and/or is internalized by atarget cell type that expresses a marker in vivo. The methods typicallyinvolve providing a display library (e.g., a yeast- or phage-displaylibrary); contacting a tissue compromising the cell type with members ofthe library; isolating groups of cells from the tissue using lasercapture microdissection; and recovering members of the library that bindto cells in the isolated groups. In certain embodiments, the recoveringcomprises identifying members of the library that are internalized intocells in the isolated groups. In various embodiments, the target celltype is a pathological cell or a healthy cell characteristic of aparticular tissue. In certain embodiments, the target cell type is acancer cell (e.g., a cell of a cancer selected from the group consistingof a lung cancer, a bronchus cancer, a colorectal cancer, a prostatecancer, a breast cancer, a pancreas cancer, a stomach cancer, an ovariancancer, a urinary bladder cancer, a brain or central nervous systemcancer, a peripheral nervous system cancer, an esophageal cancer, acervical cancer, a melanoma, a uterine or endometrial cancer, a cancerof the oral cavity or pharynx, a liver cancer, a kidney cancer, abiliary tract cancer, a small bowel or appendix cancer, a salivary glandcancer, a thyroid gland cancer, an adrenal gland cancer, anosteosarcoma, a chondrosarcoma, a liposarcoma, a testicular cancer, anda malignant fibrous histiocytoma). In certain embodiments the methodinvolves counter-selecting the library on a normal cell population toreduce or eliminate members of the library that bind to normal cells. Incertain embodiments, the providing comprises preselecting the library ona panel of tumor cell lines to create a library enriched for binders tofunctional cell surface epitopes on tumor cells. In certain embodiments,the preselecting is under internalizing conditions. In variousembodiments, the recovering comprises amplifying a nucleic acid sequenceencoding all or part of a displayed VH and/or VL domain from the boundor internalized members of the library.

Definitions

The terms “polypeptide”, “peptide” and “protein” are usedinterchangeably herein to refer to a polymer of amino acid residues. Theterms apply to amino acid polymers in which one or more amino acidresidue is an artificial chemical analogue of a corresponding naturallyoccurring amino acid, as well as to naturally occurring amino acidpolymers. The term also includes variants on the traditional peptidelinkage joining the amino acids making up the polypeptide.

The terms “nucleic acid” or “oligonucleotide” or grammatical equivalentsherein refer to at least two nucleotides covalently linked together. Anucleic acid of the present invention is preferably single-stranded ordouble stranded and will generally contain phosphodiester bonds,although in some cases, as outlined below, nucleic acid analogs areincluded that may have alternate backbones, comprising, for example,phosphoramide (Beaucage et al. (1993) Tetrahedron 49(10):1925) andreferences therein; Letsinger (1970) J. Org. Chem. 35:3800; Sprinzl etal. (1977) Eur. J. Biochem. 81: 579; Letsinger et al. (1986) Nucl. AcidsRes. 14: 3487; Sawai et al. (1984) Chem. Lett. 805, Letsinger et al.(1988) J. Am. Chem. Soc. 110: 4470; and Pauwels et al. (1986) ChemicaScripta 26: 1419), phosphorothioate (Mag et al. (1991) Nucleic AcidsRes. 19:1437; and U.S. Pat. No. 5,644,048), phosphorodithioate (Briu etal. (1989) J Am. Chem. Soc. 111:2321, O-methylphophoroamidite linkages(see Eckstein, Oligonucleotides and Analogues: A Practical Approach,Oxford University Press), and peptide nucleic acid backbones andlinkages (see Egholm (1992) J Am. Chem. Soc. 114:1895; Meier et al.(1992) Chem. Int. Ed. Engl. 31: 1008; Nielsen (1993) Nature, 365: 566;Carlsson et al. (1996) Nature 380: 207). Other analog nucleic acidsinclude those with positive backbones (Denpcy et al. (1995) Proc. Natl.Acad. Sci. USA 92: 6097; non-ionic backbones (U.S. Pat. Nos. 5,386,023,5,637,684, 5,602,240, 5,216,141 and 4,469,863; Angew. (1991) Chem. Intl.Ed. English 30: 423; Letsinger et al. (1988)J Am. Chem. Soc. 110:4470;Letsinger et al. (1994) Nucleoside & Nucleotide 13:1597; Chapters 2 and3, ASC Symposium Series 580, “Carbohydrate Modifications in AntisenseResearch”, Ed. Y. S. Sanghui and P. Dan Cook; Mesmaeker et al. (1994),Bioorganic & Medicinal Chem. Lett. 4: 395; Jeffs et al. (1994) J.Biomolecular NMR 34:17; Tetrahedron Lett. 37:743 (1996)) and non-ribosebackbones, including those described in U.S. Pat. Nos. 5,235,033 and5,034,506, and Chapters 6 and 7, ASC Symposium Series 580, CarbohydrateModifications in Antisense Research, Ed. Y. S. Sanghui and P. Dan Cook.Nucleic acids containing one or more carbocyclic sugars are alsoincluded within the definition of nucleic acids (see Jenkins et al.(1995), Chem. Soc. Rev. pp 169-176). Several nucleic acid analogs aredescribed in Rawls, C & E News Jun. 2, 1997 page 35. These modificationsof the ribose-phosphate backbone may be done to facilitate the additionof additional moieties such as labels, or to increase the stability andhalf-life of such molecules in physiological environments.

The term “biotin” refers to biotin and modified biotins or biotinanalogues that are capable of binding avidin or various avidinanalogues. “Biotin”, can be, inter alia, modified by the addition of oneor more addends, usually through its free carboxyl residue. Usefulbiotin derivatives include, but are not limited to, active esters,amines, hydrazides and thiol groups that are coupled with acomplimentary reactive group such as an amine, an acyl or alkyl group, acarbonyl group, an alkyl halide or a Michael-type acceptor on theappended compound or polymer.

Avidin, typically found in egg whites, has a very high binding affinityfor biotin, which is a B-complex vitamin (Wilcheck et al. (1988) Anal.Biochem, 171: 1). Streptavidin, derived from Streptomyces avidinii, issimilar to avidin, but has lower non-specific tissue binding, andtherefore often is used in place of avidin. As used herein “avidin”includes all of its biological forms either in their natural states orin their modified forms. Modified forms of avidin which have beentreated to remove the protein's carbohydrate residues (“deglycosylatedavidin”), and/or its highly basic charge (“neutral avidin”), forexample, also are useful in the invention. Both avidin and streptavidinhave a tetravalency for biotin, thus permitting amplification when theformer bind to biotin. In certain embodiments, four detection ortherapeutic agents, such as nuclides, can be attached to each targetingprotein.

The term “residue” as used herein refers to natural, synthetic, ormodified amino acids.

As used herein, an “antibody” refers to a protein consisting of one ormore polypeptides substantially encoded by immunoglobulin genes orfragments of immunoglobulin genes. The recognized immunoglobulin genesinclude the kappa, lambda, alpha, gamma, delta, epsilon and mu constantregion genes, as well as myriad immunoglobulin variable region genes.Light chains are classified as either kappa or lambda. Heavy chains areclassified as gamma, mu, alpha, delta, or epsilon, which in turn definethe immunoglobulin classes, IgG, IgM, IgA, IgD and IgE, respectively.

A typical immunoglobulin (antibody) structural unit is known to comprisea tetramer. Each tetramer is composed of two identical pairs ofpolypeptide chains, each pair having one “light” (about 25 kD) and one“heavy” chain (about 50-70 kD). The N-terminus of each chain defines avariable region of about 100 to 110 or more amino acids primarilyresponsible for antigen recognition. The terms variable light chain (VL)and variable heavy chain (VH) refer to these light and heavy chainsrespectively.

Antibodies exist as intact immunoglobulins or as a number of wellcharacterized fragments produced by digestion with various peptidases.Thus, for example, pepsin digests an antibody below the disulfidelinkages in the hinge region to produce F(ab)′₂, a dimer of Fab whichitself is a light chain joined to V_(H)-C_(H)1 by a disulfide bond. TheF(ab)′₂ may be reduced under mild conditions to break the disulfidelinkage in the hinge region thereby converting the (Fab′)₂ dimer into aFab′ monomer. The Fab′ monomer is essentially a Fab with part of thehinge region (see, Fundamental Immunology, W. E. Paul, ed., Raven Press,N.Y. (1993), for a more detailed description of other antibodyfragments). While various antibody fragments are defined in terms of thedigestion of an intact antibody, one of skill will appreciate that suchFab′ fragments may be synthesized de novo either chemically or byutilizing recombinant DNA methodology. Thus, the term antibody, as usedherein also includes antibody fragments either produced by themodification of whole antibodies or synthesized de novo usingrecombinant DNA methodologies. Preferred antibodies include single chainantibodies (antibodies that exist as a single polypeptide chain), morepreferably single chain Fv antibodies (sFv or scFv) in which a variableheavy and a variable light chain are joined together (directly orthrough a peptide linker) to form a continuous polypeptide. The singlechain Fv antibody is a covalently linked V_(H)-V_(L) heterodimer whichmay be expressed from a nucleic acid including V_(H)- and V_(L)-encodingsequences either joined directly or joined by a peptide-encoding linker.Huston, et al. (1988) Proc. Nat. Acad. Sci. USA, 85: 5879-5883. Whilethe V_(H) and V_(L) are connected to each as a single polypeptide chain,the V_(H) and V_(L) domains associate non-covalently. The firstfunctional antibody molecules to be expressed on the surface offilamentous phage were single-chain Fv's (scFv), however, alternativeexpression strategies have also been successful. For example Fabmolecules can be displayed on phage if one of the chains (heavy orlight) is fused to g3 capsid protein and the complementary chainexported to the periplasm as a soluble molecule. The two chains can beencoded on the same or on different replicons; the important point isthat the two antibody chains in each Fab molecule assemblepost-translationally and the dimer is incorporated into the phageparticle via linkage of one of the chains to, e.g., g3p (see, e.g., U.S.Pat. No. 5,733,743). The scFv antibodies and a number of otherstructures converting the naturally aggregated, but chemically separatedlight and heavy polypeptide chains from an antibody V region into amolecule that folds into a three dimensional structure substantiallysimilar to the structure of an antigen-binding site are known to thoseof skill in the art (see e.g., U.S. Pat. Nos. 5,091,513, 5,132,405, and4,956,778). Particularly preferred antibodies should include all thathave been displayed on phage (e.g., scFv, Fv, Fab and disulfide linkedFv (Reiter et al. (1995) Protein Eng. 8: 1323-1331).

The term “specifically binds”, as used herein, when referring to abiomolecule (e.g., protein, nucleic acid, antibody, etc.), refers to abinding reaction that is determinative of the presence biomolecule inheterogeneous population of molecules (e.g., proteins and otherbiologics). Thus, under designated conditions (e.g. immunoassayconditions in the case of an antibody or stringent hybridizationconditions in the case of a nucleic acid), the specified ligand orantibody binds to its particular “target” molecule and does not bind ina significant amount to other molecules present in the sample.

An “effector” refers to any molecule or combination of molecules whoseactivity it is desired to deliver/into and/or localize at cell.Effectors include, but are not limited to labels, cytotoxins, enzymes,growth factors, transcription factors, drugs, etc.

A “reporter” is an effector that provides a detectable signal (e.g. is adetectable label). In certain embodiments, the reporter need not providethe detectable signal itself, but can simply provide a moiety thatsubsequently can bind to a detectable label.

The term “conservative substitution” is used in reference to proteins orpeptides to reflect amino acid substitutions that do not substantiallyalter the activity (specificity or binding affinity) of the molecule.Typically, conservative amino acid substitutions involve substitution ofone amino acid for another amino acid with similar chemical properties(e.g. charge or hydrophobicity). The following six groups each containamino acids that are typical conservative substitutions for oneanother: 1) Alanine (A), Serine (S), Threonine (T); 2) Aspartic acid(D), Glutamic acid (E); 3) Asparagine (N), Glutamine (Q); 4) Arginine(R), Lysine (K); 5) Isoleucine (I), Leucine (L), Methionine (M), Valine(V); and 6) Phenylalanine (F), Tyrosine (Y), Tryptophan (W).

The terms “epitope tag” or “affinity tag” are used interchangeablyherein, and used refers to a molecule or domain of a molecule that isspecifically recognized by an antibody or other binding partner. Theterm also refers to the binding partner complex as well. Thus, forexample, biotin or a biotin/avidin complex are both regarded as anaffinity tag. In addition to epitopes recognized in epitope/antibodyinteractions, affinity tags also comprise “epitopes” recognized by otherbinding molecules (e.g. ligands bound by receptors), ligands bound byother ligands to form heterodimers or homodimers, His₆ bound by Ni-NTA,biotin bound by avidin, streptavidin, or anti-biotin antibodies, and thelike.

Epitope tags are well known to those of skill in the art. Moreover,antibodies specific to a wide variety of epitope tags are commerciallyavailable. These include but are not limited to antibodies against theDYKDDDDK (SEQ ID NO:2) epitope, c-myc antibodies (available from Sigma,St. Louis), the HNK-1 carbohydrate epitope, the HA epitope, the HSVepitope, the His₄, His₅, and His₆ epitopes that are recognized by theHis epitope specific antibodies (see, e.g., Qiagen), and the like. Inaddition, vectors for epitope tagging proteins are commerciallyavailable. Thus, for example, the pCMV-Tag1 vector is an epitope taggingvector designed for gene expression in mammalian cells. A target geneinserted into the pCMV-Tag1 vector can be tagged with the FLAG® epitope(N-terminal, C-terminal or internal tagging), the c-myc epitope(C-terminal) or both the FLAG (N-terminal) and c-myc (C-terminal)epitopes.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 schematically illustrates one embodiment, of a method ofselecting antibodies according to the present invention. The naïve phageantibody library was first counterselected on a panel of non-tumorigeniccell lines to remove binders to common cell surface antigens (not shown)and then selected on live tumor cells under internalizing conditions togenerate a sublibrary that is enriched for binders to internalizing cellsurface epitopes. Further selection of this sublibrary on tissue slidesby LCM enriched scFv fragments that bind to tumor cells in situ.Monoclonal phage antibodies were identified by screening selectionoutput on tumor cell lines followed by rescreening positive clones ontissue slides. This selection scheme effectively restricts selectionoutcomes to phage antibodies that bind to epitopes present on both tumorcell lines and tumor cells in situ from actual cases. Moreover theseantibodies are expected to possess internalizing functions that can beexploited for targeted payload delivery.

FIG. 2 illustrates selection of phage antibody library on tissue slidesby LCM. Tissue pieces containing tumor cells and tumor-bound phage wereprocured by Leica AS LMD and collected on the cap of a PCR tube (step1). scFv-coding regions were amplified by PCR (step 2) and spliced intoa phage display vector to create LCM secondary libraries (step 3) thatwere used for screening (step 4) or additional rounds of selection (step5). Ctr, control; MW, molecular weight.

FIG. 3 illustrates initial screening of selection output. FACS analysiswas performed on tumor cell lines to identify positive clones,restricting the number of phage antibody that needed to be screened ontissue slides. Ctr, helper phage. Clones 1-4, four positive clonesrandomly chosen from the output following one round of LCM-basedselection. Because these antibodies bound to both PC3 and Du-145 cells,it is likely that they bind to tumor antigens instead of artifactsassociated with slide preparation. Tumor specificity and clinicalrelevance were further studied by IHC. PE-A, phycoerythrin channel;FITC-A, FITC channel.

FIG. 4 , panels A-C, show the results of immunohistochemistry studies.Biotinylated scFv fragments were used to stain CaP tissues. The UA20scFv was originally isolated from selection on paraffin-embeddedtissues; it stained tumor cells in both frozen and paraffin-embeddedtissue slides. The 585II41 scFv was originally isolated from selectionon frozen tissues; it stained tumor cells in frozen but notparaffin-embedded tissue slides. Panel A: staining of frozen tissueswith UA20 scFv. Panel B: staining of frozen tissues with 585II41 scFv.Panel C: staining of paraffin-embedded CaP tissues with UA20 scFv.

FIGS. 5A, 5B, 5C illustrate the internalization of immunoliposomes.Fluorescent liposomes conjugated with the UA20 scFv were tested forinternalization into prostate cancer cells. FIG. 5A: microscopicexamination of uptake of UA20-ILs by PC3 and Du-145 cells. There was nouptake by BPH-1 cells. 5B: FACS analysis of uptake ofUA20-DiIC18(3)-DS-ILs by Du-145 cells. MFI, mean fluorescence intensity.FIG. 5C: quantification of UA20 scFv-IL uptake by prostate cancer andcontrol cells. MFI values were obtained from FACS. NT-LPs, non-targetedliposomes.

FIGS. 6A and 6B illustrate the identification of ALCAM/MEMD/CD166 as thetarget of the 585II41 scFv. FIG. 6A shows that binding of the 585II41scFv to prostate cancer cells was specifically competed by a previouslyidentified anti-ALCAM scFv, H3, and its corresponding IgG1 but not by acontrol scFv, OA12, and its corresponding IgG1. FIG. 6B illustratesanalysis of IP products by Western blot. Lysates from biotinsurface-labeled Du-145 cells were incubated with 585II41 scFv and OA12scFv (control) to generate IP products that were analyzed by Westernblot using an ALCAM-specific commercial monoclonal antibody. Only the585II41 scFv IP product reacted with the anti-ALCAM mAb. The band(indicated by an arrow) is located between 100 and 110 kDa. ALCAM ispredicted to be a 65-kDa protein, but glycosylation causes it to appearas a band of ˜105 kDa on SDS-PAGE, consistent with previous reports(Saifullah et al. (2004) J Immunol. 173: 6125-6133). MFI, meanfluorescence intensity

FIG. 7 shows the amino acid sequences of internalizing prostate cancerspecific antibodies: 3051.1 (SEQ ID NO:3), G12FC3 (SEQ ID NO:4), M6c42b(SEQ ID NO:5), 4F3YW (SEQ ID NO:6), M40pr146 (SEQ ID NO:7), UA20 (SEQ IDNO:8), UA8 (SEQ ID NO:9), 585II41 (SEQ ID NO:10), 585II41.1 (SEQ IDNO:11), 585II56 (SEQ ID NO:12), 3076 (SEQ ID NO:13), and 3051 (SEQ IDNO:14).

FIG. 8 shows the amino acid sequences of internalizing prostate cancerspecific antibodies: M49R (SEQ ID NO:15), RCI-14 (SEQ ID NO:16), I179_4(SEQ ID NO:17), I179_3 (SEQ ID NO:18), T5II-4B.1 (SEQ ID NO:19),T5II-4B.2 (SEQ ID NO:20), RCI-11 (SEQ ID NO:21), RCI-20 (SEQ ID NO:22),CI-11A (SEQ ID NO:23), CI-14A (SEQ ID NO:24), and S95-2 (SEQ ID NO:25).

FIG. 9 shows the results of SPECT/CT imaging of UA20 scFv targeting toprostate cancer Du-145 xenograft tumor (arrow) in nude mice.

FIGS. 10A, and 10B show the results of biodistribution studies. FIG.10A: Biodistribution study. The values of % ID/g tissue for both theUA20 scFv and the control N3M2 scFv were plotted for tumor, blood andother organs/tissues. Standard errors are indicated. Sm.Int., smallintestine. Lg.Int., large intestine. FIG. 10B: The ratio of % ID/gtissue (UA20 scFv over control N3M2 scFv) was plotted.

FIG. 11 shows the results of a measurement of apparent dissociationequilibrium constant (KD) of the anti-ALCAM IgG1 (585II41.1, an H3variant) on prostate cancer Du-145 cells by FACS. Monodispersed DU-145cells were incubated with varying concentrations of IgG1s at 4° C.overnight to allow equilibrium binding. After washing, bound human IgG1swere detected by R-phycoerythrin-conjugated goat anti-human secondaryantibody and analyzed by FACS. Mean fluorescence intensity (MFI) valueswere plotted and the KD was determined by curve fitting using GraphPad(GraphPad Software, San Diego, CA).

DETAILED DESCRIPTION

Much work has been done to develop tumor-targeting antibodies byselecting a phage antibody library on cancer cell lines. When tumorcells are removed from their natural environment, however, they mayundergo genetic and epigenetic changes yielding different surfaceantigens than those seen in actual cases of cancer. In one embodiment,this invention pertains to a method that allows selection of phageantibodies against tumor cells in situ on fresh, fresh frozen, andparaffin-embedded tissues using laser capture microdissection. Lasercapture microdissection (LCM) allows small clusters of homogenous cellsto be isolated and removed from tissue sections under direct microscopicvisualization. It was a surprising discovery that it is possible toexploit this technology for the selection of phage binding specificallyto certain target (e.g., tumor) cells while ignoring adulteratingentities such as non-neoplastic cells and stromal elements and that theresulting methods can be used to isolate, e.g., cancer cell specificantibodies that are internalized by the target cell(s).

Using the methods described herein, a number of antibodies wereidentified that target clinically represented prostate cancer antigens.We identified AL-CAM/MEMD/CD166, a newly discovered prostate cancermarker, as the target for one of the selected antibodies, demonstratingthe effectiveness of the approach. We further conjugated two singlechain Fv fragments to liposomes and demonstrated that thesenanotargeting devices were efficiently delivered to the interior ofprostate cancer cells. The ability to deliver payload intracellularlyand to recognize tumor cells in situ makes these antibodies attractivecandidates for the development of targeted cancer therapeutics.

I. Selecting Phage Antibody Library on Cells in Situ Using Laser CaptureMicrodissection (LCM).

Much work has been done to develop tumor-targeting antibodies byselecting a phage antibody library on cancer cell lines. However, whentumor cells are removed from their natural environment, they may undergogenetic and epigenetic changes yielding different surface antigens thanthose seen in actual cases of cancer.

We developed a strategy that allows selection of phage antibodiesagainst tumor cells in situ, for example, of fresh samples, on frozenand paraffin-embedded tissues, and the like using laser capturemicrodissection (see, e.g., FIGS. 1 and 2 ). In various embodiments themethods involve providing a display library (e.g., a yeast- orphage-display library), contacting a tissue compromising the target typewith members of the library; isolating groups of cells from the tissueusing laser capture microdissection; and recovering members of thelibrary that bind to cells in the isolated groups.

While the selection methods are described with respect to tumorcells/tissues, it will be recognized that using the LCM methodsdescribed herein, libraries can be used to screen for markers expressedin situ on essentially any desired cell type. Thus, for example, binders(e.g., antibodies) specific for any pathological cell type, where thepathological cell displays different markers, than other cells, can beidentified.

Methods of providing display libraries (e.g., phage display,yeast-display, and the like) are well known to those of skill in the art(see, e.g., Boder et al. (1997) Nat. Biotechnol. 15: 553-557; Liu et al.(2004) Cancer Res. 64: 704-710; Poul et al. (2000) J Mol. Biol. 301:1149-1161; U.S. Pat. Nos. 6,699,658, and 6,696,251, and the like).

The display library can optionally be counter selected on cells forwhich binding is not desired (e.g., normal healthy cells) and/orpre-selected, e.g., on a panel of target cells to enhance therepresentation of binders and/or internalizing members in the library.In one illustrative embodiment, the library is created by selecting,e.g., a naïve phage antibody display library on a panel of target cells(e.g., tumor cell lines), and where internalization is desired, underinternalizing conditions. Methods of preparation and selection of aphage antibody display library have been described, for example by Liuet al. (2004) Cancer Res. 64: 704-710, and Poul et al. (2000) J. Mol.Biol. 301: 1149-1161). In one illustrative example, (see, e.g.,Example 1) the phage library is preincubated with a panel ofnon-tumorigenic cells including, for example BPH-1, human mammaryepithelial cells, MCF10A, and human fibroblasts to remove binders tocommon cell surface antigens. The predepleted library can then,optionally be incubated with a panel of target cells (e.g., prostatecancer cell lines (PC3 and Du-145)) at 37° C. for 2 h; washed twice with100 mM glycine, pH 2.8, in the presence of 150 mM NaCl; and washed oncewith PBS, pH 7.0. Internalized phage can be recovered by lysing thecells with 100 mM triethylamine, propagated in TG1, and purified byprecipitation with polyethylene glycol 8000 as described previously (1),thereby creating a sublibrary that is enriched for binders tointernalizing cell surface molecules.

The library can then be incubated (selected against) one or more tissuescontaining the target cells. Thus, for example, selections can beperformed, on fresh, frozen, and/or paraffin embedded tissues. Forselection on slides, for example, sections of the target tissue can beplaced on microscope slides, and incubated with the library, for ½ toseveral hours, for example, at room temperature (e.g., 1 hour at roomtemperature). The tissue is then washed to remove unbound librarymembers and prepared for laser capture microdissection according tostandard methods.

Methods of performing laser capture microdissetion (LCM) are well knownto those of skill in the art. The LCM technique is generally describedby Emmert-Buck et al., (1996) Science 274: 998. In a typically LCMmethod, a transfer surface is placed onto the tissue section and thenfocally bonded to the targeted tissue, allowing it to be selectivelyremoved for later analysis. In the microscope, the operator views thetissue and selects microscopic clusters of cells for analysis, thenactivates a laser within the microscope optics. The pulsed laser beam isabsorbed within a precise spot on the transfer film immediately abovethe targeted cells. At this precise location, the film melts and fuseswith the underlying cells of choice. When the film is removed, thechosen cells remain bound to the film, while the rest of the tissue isleft behind. Manual, automated, as well as non-contact methods of LCMare well known and described, for example in U.S. Pat. Nos. 7,027,133,6,897,038, 6,870,625, 6,690,470, and 6,469,779 (see, also, Murray andCurran (eds) (2005) Laser Capture Microdissection: Methods andProtocols, Humana Press, Inc. N.J.).

Typically 5-500, more typically 100 or 200, still more typically 20-100or 20-50 cells are procured at a time, e.g., by generating a closedlaser path around the group of cells of interest. The cells can then becollected (e.g., dropped into collection tubes by electrostatic forceand gravity), and the bound and/or internalized library membersrecovered.

It was noted that phage bound to LCM-procured tissue pieces appear tolose the ability to infect bacteria, thereby posing a challenge tolibrary selection. Little bacterial growth was observed under variousculture conditions. This phenomenon was seen even in manually dissectedtissue pieces that were not exposed to the UV laser used in the LeicaLMD system. Exposure to ethanol during slide preparation for LCM seemsto be a factor contributing to the observed reduction in phageviability.

Accordingly in certain embodiments the problem is circumvented by usingthe genomes of phages (or yeast) bound to the procured cancer cellpieces as templates for amplification of scFv genes, e.g., by PCR. Theamplified scFv genes can easily be identified and/or sequenced.

The foregoing methods are intended to be illustrative an not limiting.Using the teaching provided herein other methods utilizing LCM in thescreening and selection of binding libraries in situ will be availableto one of skill in the art.

II. Internalizing Prostate Specific Antibodies.

In certain embodiments this invention provides a number of antibodiesthat specifically bind and are internalized into human prostate cancercells. The antibodies were identified by selecting human antibody genediversity libraries directly on the surface of prostate cancer cells invivo using laser microdissection methods as described above and in theexamples. Antibodies were identified that specifically bind and enterprostate cancer cells, with little or no binding to control cells.

For the selection process, the antibodies in the library were expressedas single chain Fv (scFv) antibodies comprising a variable heavy (V_(H))region linked to a variable light (V_(L)) region by a peptide linker,although it will be recognized that using the antibody sequencepresented herein other forms of the antibodies can be provided.

Representative antibodies (e.g. V_(H) and V_(L) domains) are illustratedin Tables 1 and 2, respectively as well as in FIGS. 7 and 8 .

TABLE 1 Amino acid sequences of variable heavy (VH) chain ofprostate cancer specific internalizing antibodies. Heavy chain FrameFrame Frame Frame Clone 1 CDR1 2 CDR2 3 CDR3 4 3051.1 QVQLQESGG SYGMWVRQAP TLSRS RFTISR IAVA WGO GLVKPGGPL Y GKGLEW GSGTY DNSKNT GNYF GTLRLSCAASGF (SEQ VS YADSV LYLQMN DY VTV TFS ID (SEQ KG SLRAED (SEQ SS(SEQ ID NO: ID (SEQ TAVYYC ID (SEQ NO: 26) 27) NO: ID AS NO: ID 28) NO:(SEQ 31) NO: 29) ID NO: 32) 30) G12FC3 QVQLVQSGG GSGM WVRQAP MIWYDRFTISR DKGV WGL GVVQPGRSL H GKGLEW GSNKE DNSKNT RSMD GTT RLSCAATGI (SEQVT YADSV LYLQMD V VTV PES ID (SEQ KG SLRAED (SEQ SS (SEQ ID NO: ID (SEQTAVYFC ID (SEQ NO: 33) 34) NO: ID AR NO: ID 35) NO: (SEQ 38) NO: 36)ID NO: 39) 37) M6c42b QVQLQESGG TYAM WVRQTS GIGVS RFTISR KSST WGRGLVQPGGSL R GKGLEW GDAYY DNSKNT TSND GTL RLSCSASGF (SEQ VS TDSVR LYLQMNY VTV TFG ID (SEQ G TLRAED (SEQ SS (SEQ ID NO: ID (SEQ TATYYC ID (SEQNO: 40) 41) NO: ID TR NO: ID 42) NO: (SEQ 45) NO: 43) ID NO: 46) 44)4F3YW QVQLQESGG SYAM WVRQAP VISYD RFTISR FSSG WGQ GLVQPGGSL H GKGLEWGSNKY DNSKNT WYYF GTL RLSCAASGF (SEQ VA YADSV LYLQMN DY VTV TFS ID (SEQKG SLRAED (SEQ SS (SEQ ID NO: ID (SEQ TAVYYC ID (SEQ NO: 47) 48) NO: IDAR NO: ID 49) NO: (SEQ 52) NO: 50) ID NO: 53) 51) M40pr146 QVQLLQSGGSYAM WVRQAP AISGS RFTISR SHDY WGQ GLVQPGGSL S GKGLEW GGSTY DNSKNT GDYAGTL RLSCAASGF (SEQ VS YTDSV LYLQMN GFDY VTV TFS ID (SEQ KG SLRAED (SEQSS (SEQ ID NO: ID (SEQ TAVYYC ID (SEQ NO: 54) 55) NO: ID AK NO: ID 56)NO: (SEQ 59) NO: 57) ID NO: 60) 58) UA20 QVQLQESGG NAWM WVRQAP RIKSKRFSISR TKGL LGQ GLVKPGGSL N GKGLEW TDEGT DDSKNT GGSK GTL RLSCAASGF (SEQVG TDYAA LYLQMN (SEQ VTV TFS ID (SEQ PVKG SLKTED ID SS (SEQ ID NO: ID(SEQ TGVYYC NO: (SEQ NO: 61) 62) NO: ID TA 66) ID 63) NO: (SEQ NO: 64)ID NO: 67) 65) UA8 QVOLVESGG SFGM WVRRAP VISYD RFTISR RPGG WGQ GVVQPGRSLH GKGLEW GSNQY DNSKNT GYAS GTP RLSCAASGF (SEQ VA YADSV LYLQMN GSTV VTVTFS ID (SEQ KG SLRAED AY SS (SEQ ID NO: ID (SEQ TAVYYC (SEQ (SEQ NO: 68)69) NO: ID GS ID ID 70) NO: (SEQ NO: NO: 71) ID NO: 73) 74) 72) 585II41QVQLVESGG SYAM WVRQAP AISGS RFTISR RSLI WGQ GLVQPGGSL G GKGLEW GGSTYDNSKDT DY GTL RLSCAASGF (SEQ VS YADSV LYLQMN (SEQ VTV TFS ID (SEQ KGSLRAED ID SS (SEQ ID NO: ID (SEQ TAVYYC NO: (SEQ NO: 75) 76) NO: ID AS80) ID 77) NO: (SEQ NO: 78) ID NO: 81) 79) 585II41.1 QVQLVESGG SYAMWVRQAP AISGS RFTISR RSLL WGQ GLVQPGGSL S GKGLEW GGSTY DNSKDT DY GTLRLSCAASGF (SEQ VS YADSV LYLQMN (SEQ VTV TFS ID (SEQ KG SLRAED ID SS(SEQ ID NO: ID (SEQ TAVYYC NO: (SEQ NO: 82) 83) NO: ID AS 87) ID 84) NO:(SEQ NO: 85) ID NO: 88) 86) 585II56 QVQLQESGG SYAM WVRQAP AISGS RFTISRSAYT WGH GLVOLGGSL S GKGLEW GGSTY DNSKNT GGWY GTL RLSCAASGF (SEQ VSYADSV LYLQMS DY VTV TFS ID (SEQ KG SLRAED (SEQ SS (SEQ ID NO: ID (SEQTAFYYC ID (SEQ NO: 89) 90) NO: ID AN NO: ID 91) NO: (SEQ 94) NO: 92)ID NO: 95) 93) 3076 QVNLRESGG GYWM WVHPAP NIKQD RFTISR GLLS WGQGLVQPGGFL S GKGLEW GSEKF DNAKNS DY GTL RLSCAAFGF (SEQ VA YVDSV LFLQMN(SEQ VPV TFS ID (SEQ KG SLRAED ID SS (SEQ ID NO: ID (SEQ TAVYFC NO: (SEQNO: 96) 97) NO: ID AR 101) ID 98) NO: (SEQ NO: 99) ID NO: 102) 100) 3051QVQLQESGG SYGM WVRQAP TLSRS RFTISR IAVA WGQ GLVKPGGPL Y GKGLEW GSGTYDNSKNT GNYF GTL RLSCAASGF (SEQ VS YAESV LYFQMN EY VTV TFS ID (SEQ KGSLRAED (SEQ SS (SEQ ID NO: ID (SEQ TAVYYC ID (SEQ NO: 103) 104) NO: IDAS NO: ID 105) NO: (SEQ 108) NO: 106) ID NO: 109) 107) M49R QVQLQESGGDHYM WVRQAP YIRYD RFTISR LIAE WGQ GLVKPGESL D GKGLEW GSTKY DNSKNT AEGWGTL RLSCAASGF (SEQ VA YADSV LYLQMN FDP VTV TFS ID (SEQ KG SLRPED (SEQ SS(SEQ ID NO: ID (SEQ TAFYYC ID (SEQ NO: 110) 111) NO: ID AR NO: ID 112)NO: (SEQ 115) NO: 113) ID 116) NO: 114) RCI-14 QVQLLQSAG TYAM WVRQAPGISGS RFTISR DYGS WGQ GLVQPGGSL N GKGLEW GGSTN DSSKNT GWYD GTL RLSCAASGF(SEQ VS YADSV LFLQMN Y VTV TFS ID (SEQ KG SLRAED (SEQ SS (SEQ ID NO: ID(SEQ TAVYYC ID (SEQ NO: 117) 118) NO: ID AK NO: ID 119) NO: (SEQ 122)NO: 120) ID NO: 123) 121) II79_4 QVQLVESGG SYAM WVHQAP AISGS RFTISR TYYGLGQ GLVQPGGSL S GKGLEW GGSTY DNSKNT FWSG GTL RLSCAASGF (SEQ VS YADSVLYLQMN YYDY VTV TFS ID (SEQ KG SLRAED (SEQ SS (SEQ ID NO: ID (SEQ TAVYYCID (SEQ NO: 124) 125) NO: ID AK NO: ID 126) NO: (SEQ 129) NO: 127)ID NO: 130) 128) II79_3 QVQLLESGG NYAI WVRQAA GISGS RFTVSR NGGG WGQGVVQPGTSL N GKGLEW GVSTS DNSKNT PEYL GTL RLSCAASGF (SEQ VS YADSV LYLQMNQH VTV TES ID (SEQ KG SLRVED (SEQ SS (SEQ ID NO: ID (SEQ TALYYC ID (SEQNO: 131) 132) NO: ID AK NO: ID 133) NO: (SEQ 136) NO: 134) ID NO: 137)135) T5II-4B.1 QVQLQESGG SYAM WVRQAP TISGS RFTISR GAYS WGQ TLVQPGGSL SGRGLEW GGSTY DNSKNT GSY GTL RLSCAASGE (SEQ VS YADSV LYLQMN (SEQ VTV TFSID (SEQ KG SLRAED ID SS (SEQ ID NO: ID (SEQ TAVYYC NO: (SE NO:138) 139)NO: ID AK 143) Q 140) NO: (SEQ ID 141) ID NO: NO: 142) 144) T5II-4B.2QVQLQESGG SYAM WVRQAP TISGS RFTISR GAYS WGQ TLVQPGGSL S GRGLEW GGSTYDNSKNT GSH GTL RLSCAASGF (SEQ VS YADSV LYLQMN (SEQ VTV TFS ID (SEQ KGSLRAED ID SS (SEQ ID NO: ID (SEQ TAVYYC NO: (SEQ NO: 145) 146) NO: ID AK150) ID 147) NO: (SEQ NO: 148) ID NO: 151) 149) RCI-11 QVQLVESGA SYGIWVRQAP WISAY RVTMTT PIYD WGQ EVKKPGASV S GOGLEW NGNTN DTSTST SSGY GTMKVSCKASGY (SEQ MG YAQKL AYMELR DAFD VTV TFT ID (SEQ QG SLRSDD I SS(SEQ ID NO: ID (SEQ TAVYYC (SEQ (SEQ NO: 152) 153) NO: ID AR ID ID 154)NO: (SEQ NO: NO: 155) ID NO: 157) 158) 156) RCI-20 QVQLVESGG SYAM WVRQAPVISYD RFTISR PSDS WGQ GLVKPGGSL H GKGLEW GSNKY DNSKNT GWSF GTL RLSCAASGF(SEQ VA YADSV LYLQMN EH VPV TFS ID (SEQ KG SLRAED (SEQ SS (SEQ ID NO: 1ID (SEQ TAVYFC ID (SEQ NO:159) 60) NO: ID VR NO: ID 161) NO: (SEQ 164)NO: 162) ID NO: 165) 163) CI-11A QVQLQESGG SYAM WVRQAP VISYD RFTISR GDRSWGQ GLVQPGGSL S GKGLEW GSNKY DNSKNT YGAE GTL RLSCAASGF (SEQ VA YADSVLYLQMN YFQH VTV TFS ID (SEQ KG SLRAED (SEQ SS (SEQ ID NO: ID (SEQ TAVYYCID (SEQ NO: 166) 167) NO: ID VR NO: ID 168) NO: (SEQ 171) NO: 169)ID NO: 172) 170) CI-14A QVQLQESGG SYAM WVRQAP AIGGN RFTISR EGEQ WGQGLVKPGGSL H GKGLEY GGTYY DNSKNT WLEY GTT RLSCAASGF (SEQ VS ADSVK LYLQMNRYYY VTV TSS ID (SEQ G SLRAED GMDV SS (SEQ ID NO: ID (SEQ TAVYYC (SEQ(SEQ NO: 173) 174) NO: ID AK ID ID 175) NO: (SEQ NO: NO: 176) ID NO:178) 179) 177) S95-2 QVQLVESGG SYGM WVRQAP VISYD RFTISR GGRY WGQGVVQPGRSL H GKGLEW GSNKY DNSKNT SSNW GTT RLSCTASGE (SEQ VA YADSV LYLQMNFSYY VTV TES ID (SEQ KG SLRAED YYGM SS (SEQ ID NO: ID (SEQ TAVYYC DV(SEQ NO: 180) 181) NO: ID AR (SEQ ID 182) NO: (SEQ ID NO: 183) ID NO:NO: 186) 184) 185)

TABLE 2 Amino acid sequences of variable light (VL) chain ofprostate cancer specific internalizing antibodies. Light Chain FrameFrame Frame Frame Clone 1 CDR1 2 CDR2 3 CDR3 4 3051.1 SYVLTQDPA QGDSWYQERP YGKN GIPDRES QVWD FGGG VSVALGQTV LRSY GQAPLL NRPS GSNSGST SINETKVT RITC YAS VI (SEQ ATLTISR QVV VL (SEQ ID (SEQ (SEQ ID VEAGDEG (SEQ(SEQ NO: 187) ID ID NO: NO: DYYC ID ID NO: 189) 190) (SEQ ID NO: NO:188) NO: 191) 192) 193) G12FC3 NEMLTQPPS DGYS WYQQKP HDDS GIPERFS QAWDFGGG VSVAPGQTA IRTK GQAPVV DRPS GSNSGTT SISE TKLT KITC SVH VV (SEQATLTISR EVV VL (SEQ ID (SEQ (SEQ ID VEAGDEA (SEQ (SEQ NO: 194) ID ID NO:NO: DYYC ID ID NO: 196) 197) (SEQ ID NO: NO: 195) NO: 198) 199) 200)M6c42b SYVLTQDPA QGDN WYQQKP YDDS GIPERFS QAWD FGGG VSVALGQTV IGSKGQAPVL DRPS GSNSGTT SISE TKVT RITC SVH VV (SEQ ATLTISS HVI VL (SEQ ID(SEQ (SEQ ID VEAGDEA (SEQ (SEQ NO: 201) ID ID NO: DYYC ID ID NO: NO:204) (SEQ ID NO: NO: 202) 203) NO: 205) 206) 207) 4F3YW DIQMTOSPS RASHWYQQKP YAAS GVPSRES QQLG FGGG FLSASVGDR DISS GKAPKP TLQS GSGSGTE SYPLTKLE ITITC YFA LI (SEQ FTLTISS T IK (SEQ ID (SEQ (SEQ ID LQPEDFA (SEQ(SEQ NO: 208) ID ID NO: TYYC ID ID NO: NO: 211) (SEQ ID NO: NO: 209)210) NO: 212) 213) 214) M40pr146 HVILTQDPA QGDS WYQQKP YGKN GIPDRES HSRDFGGG VSVALGQTV LKSY GQAPVL NRPS GSSSGTT SSGT TKLT RITC YAS VI (SEQASLTITG HLRV VL (SEQ ID (SEQ (SEQ ID AQAEDEA (SEQ (SEQ NO: 215) ID IDNO: DYYC ID ID NO: NO: 218) (SEQ ID NO: NO: 216) 217) NO: 219) 220) 221)UA20 QSVLTQPPS SGSS WSRQLP YSND GVPDRES GTWD FGTG ASGTPGQRV SNIG GTAPKLQRPS GSKSGTS SSLS TKLT TISC NNTV LI (SEQ ASLAITG AYV VL (SEQ ID N (SEQID LOPEDEA (SEQ (SEQ NO: 222) (SEQ ID NO: DYYC ID ID ID NO: 225) (SEQ IDNO: NO: NO: 224) NO: 226) 227) 228) 223) UA8 SSELTQDPA QGDS WYQQKP YGQNGIPDRES HSRD FGVG VSVALGQTV LRSY GQAPLL IRPS GSSSGNS SSGK TKVT RITC YASVI (SEQ ASLTITG YV VL (SEQ ID (SEQ (SEQ ID AQAEDEA (SEQ (SEQ NO: 229) IDID NO: DYYC ID ID NO: NO: 232) (SEQ ID NO: NO: 230) 231) NO: 233) 234)235) 585II41 NEMLTQDPA QGDS WYQQKP YGKN GIPDRES NSRD FGGG VSVALGQTV LRSYGQAPLL NRPS GSSSGNT SSGN TKVT RITC YAS VI (SEQ ASLTITG PV VL (SEQ ID(SEQ (SEQ ID AQAEDEA (SEQ (SEQ NO: 236) ID ID NO: DYYC ID ID NO: NO:239) (SEQ ID NO: NO: 237) 238) NO: 240) 241) 242) 585II41.1 NFMLTQDPAQGDS WYQQKP YGKN GIPDRES NSRD FGGG VSVALGQTV LRSY GQAPLL NRPS GSSSGNTSSGN TKVT RITC YAS VI (SEQ ASLTITG PV VL (SEQ ID (SEQ (SEQ ID AQAEDEA(SEQ (SEQ NO: 243) ID ID NO: DYYC ID ID NO: NO: 246) (SEQ ID NO: NO:244) 245) NO: 247) 248) 249) 585II56 SSELTODPA QGDS WYQQRP YGEN GIPDRESNSRD FGGG VSVALGQTV LRTY GQAPVL SRPS GSSSGNT SSGN TKLT KITC YAS VI (SEQASLTITG HLRV VL (SEQ ID (SEQ (SEQ ID AQAEDEA (SEQ (SEQ NO: 250) ID IDNO: DYYC ID ID NO: NO: 253) (SEQ ID NO: NO: 251) 252) NO: 254) 255) 256)3076 NFMLTOPPS GGYN WYQQKP HDDS GIPERFS QAWD FGGG VSVAPGKTA IGTK GQAPVVDRPS GSNSGTT SISE TKLT SLTC SVH VV (SEQ ATLTIIR EVV VL (SEQ ID (SEQ (SEQID VEAGDEA (SEQ (SEQ NO: 257) ID ID NO: DYYC ID ID NO: NO: 260) (SEQ IDNO: NO: 258) 259) NO: 261) 262) 263) 3051 SYVLTQDPA QGDS WYQERP YGKNGIPDRES QVWD FGGG VSVALGQTV LRSY GQAPLL NRPS GSNSGST SINE TKVT RITC YASVI (SEQ ATLTISR QVV VL (SEQ ID (SEQ (SEQ ID VEAGDEG (SEQ (SEQ NO: 264)ID ID NO: DYYC ID ID NO: NO: 267) (SEQ ID NO: NO: 265) 266) NO: 268)269) 270) M49R NFMLTOPPS GGNN WYQQKP YDDS GIPERFS QVWD FGGG VSVAPGKTAIGSK GQAPVL DRPS GSNSGNT SSSD TKVT RITC SVY VV (SEQ ATLTISR HVV VL(SEQ ID (SEQ (SEQ ID VEAGDEA (SEQ (SEQ NO: 271) ID ID NO: DYYC ID ID NO:NO: 274) (SEQ ID NO: NO: 272) 273) NO: 275) 276) 277) RCI-14 SSELTODPAQGDS WYQERP YGRN GIPDRES QVWD FGGG VSVALGQTV LRSY GQAPLL ERPS ASSSGNTSENE TKLT RITC YAS VI (SEQ ASLTITG QVV VL (SEQ ID (SEQ (SEQ ID AQAEDEA(SEQ (SEQ NO: 278) ID ID NO: DYYC ID ID NO: NO: 281) (SEQ ID NO: NO:279) 280) NO: 282) 283) 284) II79_4 SSELTQDPA QGDS WYQQKP YGEN GIPDRESHSRD FGGG VSVGLGQTV LRSY GQAPIL NRPS GSSSGNT SSGT TKLT TITC YAN VI (SEQASLTITG HLRV VL (SEQ ID (SEQ (SEQ ID AQAEDEA (SEQ (SEQ NO: 285) ID IDNO: DYYC ID ID NO: NO: 288) (SEQ ID NO: NO: 286) 287) NO: 289) 290) 291)II79_3 QSVLTQPPS SGSS WSRQLP YSND GVPDRES GTWD FGTG ASGTPGQRV SNIGGTAPKL QRPS GSKSGTS SSLS TKLT TISC NNTV LI (SEQ ASLAITG AYV VL (SEQ ID N(SEQ ID LOPEDEA (SEQ (SEQ NO: 292) (SEQ ID NO: DYYC ID ID ID NO: 295)(SEQ ID NO: NO: NO: 294) NO: 296) 297) 298) 293) T5II-4B.1 SSELTQDPAQGDS WYQQKP YGEN GIPDRES QAWD FGGG VSVALGQTV LRSY GQAPSL SRPS GSSSGNTSSTA TKLT RITC YAS VI (SEQ ASLTITG VV VL (SEQ ID (SEQ (SEQ ID AQAENEA(SEQ (SEQ NO: 299) ID ID NO: DYYC ID ID NO: NO: 302) (SEQ ID NO: NO:300) 301) NO: 303) 304) 305) T5II-4B.2 SSELTODPA QGDS WYQQKP YGENGIPDRES QAWD FGGG VSVALGQTV LRSY GQAPSL SRPS GSSSGNT SSTA TKLT RITC YASVI (SEQ ASLTITG VV VL (SEQ ID (SEQ (SEQ ID AQAENEA (SEQ (SEQ NO: 306) IDID NO: DYYC ID ID NO: NO: 309) (SEQ ID NO: NO: 307) 308) NO: 310) 311)312) RCI-11 DIVMTQSPS RASE WYQQKP YKAS GAPSRES QQYH FGPG TLSASIGDR GIYHGKAPKL SLAS GSGSGTD TISR TKVD VTITC WLA LI (SEQ FTLTISS T IK (SEQ ID(SEQ (SEQ ID LOPDDFA (SEQ (SEQ NO: 313) ID ID NO: TYYC ID ID NO: NO:316) (SEQ ID NO: NO: 314) 315) NO: 317) 318) 319) RCI-20 QSVLTOPPS SGSSWSRQLP YSND GVPDRES GTWD FGTG ASGTPGQRV SNIG GTAPKL QRPS GSKSGTS SSLSTKLT TISC NNTV LI (SEQ ASLAITG AYV VL (SEQ ID N (SEQ ID LQPEDEA (SEQ(SEQ NO: 320) (SEQ ID NO: DYYC ID ID ID NO: 323) (SEQ ID NO: NO: NO:322) NO: 324) 325) 326) 321) CI-11A SSELTQDPA QGDS WYQQKP YGKN GIPDRESNSRD FGGG VSVASGQTV LRSY GQAPLL IRPS GSTSGNS SSGN TKLT RITC YAS VI (SEQASLTITG RNWV VL (SEQ ID (SEQ (SEQ ID AQAEDEA (SEQ (SEQ NO: 327) ID IDNO: DYYC ID ID NO: NO: 330) (SEQ ID NO: NO: 328) 329) NO: 331) 332) 333)CI-14A SSELTODPA QGDS WYQQKP YGEN GIPDRES QAWD FGGG VSVALGQTV LRSYGQAPSL SRPS GSSSGNT SSTA TKLT RITC YAS VI (SEQ ASLTITG VV VL (SEQ ID(SEQ (SEQ ID AQAENEA (SEQ (SEQ NO: 334) ID ID NO: DYYC ID ID NO: NO:337) (SEQ ID NO: NO: 335) 336) NO: 338) 339) 340) S95-2 NFMLTOPPS GGNNWYQQKP YDDS GIPERFS QVWD FGGG VSVAPGKTA IGSK GQAPVL DRPS GSNSGNT SSSDTKVT RITC SVY VV (SEQ ATLTISR HVV VL (SEQ ID (SEQ (SEQ ID VEAGDEA (SEQ(SEQ NO: 341) ID ID NO: DYYC ID ID NO: NO: 344) (SEQ ID NO: NO: 342)343) NO: 345) 346) 347)

In certain embodiments, for single chain Fv antibodies the variableheavy (VH) region is coupled to the variable light (V_(L)) eitherdirectly, or more preferably by a peptide linker (e.g., (Gly₄Ser)₃, SEQID NO:350). Illustrative scFv antibodies are shown in Table 3.

Using the sequence information provided in Tables 1, 2, and/or 3, and/orin FIGS. 7 and 8 the antibodies 3051.1, G12FC3, M6c42b, 4F3YW, M40pr146,UA20, UA8, 585II41, 585II41.1, 585II56, 3076, 3051, M49R, RCI-14,I179_4, I179_3, T5II-4B.1, T5II-4B.2, RCI-11, RCI-20, CI-11A, CI-14A,and S95-2, or antibodies comprising one or more of the CDRs comprisingthese antibodies, or antibodies comprising the VH and/or VL domain(s) ofthese antibodies can readily be prepared using standard methods (e.g.chemical synthesis methods and/or recombinant expression methods) wellknown to those of skill in the art.

In addition, other “related” prostate cancer specific antibodies can beidentified by screening for antibodies that bind to the same epitope(e.g. that compete with the listed antibodies for binding to a prostatecancer cell) and/or by modification of the antibodies identified herein(e.g., 3051.1, G12FC3, M6c42b, 4F3YW, M40pr146, UA20, UA8, 585II41,585II41.1, 585II56, 3076, 3051, M49R, RCI-14, I179_4, I179_3, T5II-4B.1,T5II-4B.2, RCI-11, RCI-20, CI-11A, CI-14A, and/or S95-2) to producelibraries of modified antibody and then rescreening antibodies in thelibrary for improved binding to prostate cancer cells, and/or byscreening of various libraries on prostate cancer cells, e.g., asillustrated in Example 1.

TABLE 3 Illustrative scFv antibodies. The VL and VH regionsare joined by a (Gly₄Ser)₃ (SEQ ID NO: 1) linker (shown underlined).Clone Amino Acid Sequence SEQ ID No 3051.1QVQLQESGGGLVKPGGPLRLSCAASGFTFSSYGMYWVRQA 3PGKGLEWVSTLSRSGSGTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCASIAVAGNYFDYWGQGTLVTVSS G GGGSGGGGSGGGGSSYVLTQDPAVSVALGQTVRITCQGDS LRSYYASWYQERPGQAPLLVIYGKNNRPSGIPDRESGSNSGSTATLTISRVEAGDEGDYYCQVWDSINEQVVFGGGTKVT VL G12FC3QVQLVQSGGGVVQPGRSLRLSCAATGIPFSGSGMHWVRQA 4PGKGLEWVTMIWYDGSNKFYADSVKGRFTISRDNSKNTLYLQMDSLRAEDTAVYFCARDKGVRSMDVWGLGTTVTVSS GG GGSGGGGSGGGGSNFMLTQPPSVSVAPGQTAKITCDGYSI RTKSVHWYQQKPGQAPVVVVHDDSDRPSGIPERFSGSNSGTTATLTISRVEAGDEADYYCQAWDSISEEVVFGGGTKLTV L M6c42bQVQLQESGGGLVQPGGSLRLSCSASGFTFGTYAMRWVRQT 5SGKGLEWVSGIGVSGDAYYTDSVRGRFTISRDNSKNTLYLQMNTLRAEDTATYYCTRKSSTTSNDYWGRGTLVTVSS GGG GSGGGGSGGGGSSYVLTQDPAVSVALGQTVRITCQGDNIG SKSVHWYQQKPGQAPVLVVYDDSDRPSGIPERFSGSNSGTTATLTISSVEAGDEADYYCQAWDSISEHVIFGGGTKVTVL 4F3YWQVQLQESGGGLVQPGGSLRLSCAASGFTESSYAMHWVRQA 6PGKGLEWVAVISYDGSNKYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARFSSGWYYFDYWGQGTLVTVSS G GGGSGGGGSGGGGSDIQMTQSPSFLSASVGDRITITCRAS HDISSYFAWYQQKPGKAPKPLIYAASTLQSGVPSRESGSGSGTEFTLTISSLQPEDFATYYCQQLGSYPLTFGGGTKLEI K M40pr146QVQLLQSGGGLVQPGGSLRLSCAASGFTESSYAMSWVRQA 7PGKGLEWVSAISGSGGSTYYTDSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCAKSHDYGDYAGFDYWGQGTLVTVS S GGGGSGGGGSGGGGSHVILTQDPAVSVALGQTVRITCQG DSLKSYYASWYQQKPGQAPVLVIYGKNNRPSGIPDRESGSSSGTTASLTITGAQAEDEADYYCHSRDSSGTHLRVEGGGT KLTVL UA20QVQLQESGGGLVKPGGSLRLSCAASGFTFSNAWMNWVRQA 8PGKGLEWVGRIKSKTDEGTTDYAAPVKGRESISRDDSKNTLYLQMNSLKTEDTGVYYCTATKGLGGSKLGQGTLVTVSS G GGGSGGGGSGGGGSQSVLTQPPSASGTPGQRVTISCSGSS SNIGNNTVNWSRQLPGTAPKLLIYSNDQRPSGVPDRESGSKSGTSASLAITGLQPEDEADYYCGTWDSSLSAYVEGTGTK LTVL UA8QVQLVESGGGVVQPGRSLRLSCAASGFTFSSFGMHWVRRA 9PGKGLEWVAVISYDGSNQYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCGSRPGGGYASGSTVAYWGQGTPVT VSS GGGGSGGGGSGGGGSSSELTQDPAVSVALGQTVRITC QGDSLRSYYASWYQQKPGQAPLLVIYGQNIRPSGIPDRESGSSSGNSASLTITGAQAEDEADYYCHSRDSSGKYVFGVGT KVTVL 585II41QVQLVESGGGLVQPGGSLRLSCAASGFTESSYAMGWVRQA 10PGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKDTLYLQMNSLRAEDTAVYYCASRSLLDYWGQGTLVTVSS GGGGS GGGGSGGGGSNFMLTQDPAVSVALGQTVRITCQGDSLRSY YASWYQQKPGQAPLLVIYGKNNRPSGIPDRESGSSSGNTASLTITGAQAEDEADYYCNSRDSSGNPVFGGGTKVTVL 585II41.1QVQLVESGGGLVQPGGSLRLSCAASGFTESSYAMSWVRQA 11PGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKDTLYLQMNSLRAEDTAVYYCASRSLLDYWGQGTLVTVSS GGGGS GGGGSGGGGSNFMLTQDPAVSVALGQTVRITCQGDSLRSY YASWYQQKPGQAPLLVIYGKNNRPSGIPDRFSGSSSGNTASLTITGAQAEDEADYYCNSRDSSGNPVFGGGTKVTVL 585II56QVQLQESGGGLVQLGGSLRLSCAASGFTESSYAMSWVRQA 12PGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMSSLRAEDTAFYYCANSAYTGGWYDYWGHGTLVTVSS G GGGSGGGGSGGGGSSSELTQDPAVSVALGQTVKITCQGDS LRTYYASWYQQRPGQAPVLVIYGENSRPSGIPDRESGSSSGNTASLTITGAQAEDEADYYCNSRDSSGNHLRVFGGGTKL TVL 3076QVNLRESGGGLVQPGGFLRLSCAAFGFTFSGYWMSWVHPA 13PGKGLEWVANIKQDGSEKFYVDSVKGRFTISRDNAKNSLFLQMNSLRAEDTAVYFCARGLLSDYWGQGTLVPVSS GGGGS GGGGSGGGGSNFMLTQPPSVSVAPGKTASLTCGGYNIGTK SVHWYQQKPGQAPVVVVHDDSDRPSGIPERFSGSNSGTTATLTIIRVEAGDEADYYCQAWDSISEEVVFGGGTKLTVL 3051QVQLQESGGGLVKPGGPLRLSCAASGFTFSSYGMYWVRQA 14PGKGLEWVSTLSRSGSGTYYAESVKGRFTISRDNSKNTLYFQMNSLRAEDTAVYYCASIAVAGNYFEYWGQGTLVTVSS G GGGSGGGGSGGGGSSYVLTQDPAVSVALGQTVRITCQGDS LRSYYASWYQERPGQAPLLVIYGKNNRPSGIPDRESGSNSGSTATLTISRVEAGDEGDYYCQVWDSINEQVVFGGGTKVT VL M49RQVQLQESGGGLVKPGESLRLSCAASGFTFSDHYMDWVRQA 15PGKGLEWVAYIRYDGSTKYYADSVKGRFTISRDNSKNTLYLQMNSLRPEDTAFYYCARLIAEAEGWEDPWGQGTLVTVSS GGGGSGGGGSGGGGSNFMLTQPPSVSVAPGKTARITCGGN NIGSKSVYWYQQKPGQAPVLVVYDDSDRPSGIPERFSGSNSGNTATLTISRVEAGDEADYYCQVWDSSSDHVVFGGGTKV TVL RCI-14QVQLLQSAGGLVQPGGSLRLSCAASGFTFSTYAMNWVRQA 16PGKGLEWVSGISGSGGSTNYADSVKGRFTISRDSSKNTLFLQMNSLRAEDTAVYYCAKDYGSGWYDYWGQGTLVTVSS GG GGSGGGGSGGGGSSSELTQDPAVSVALGQTVRITCQGDSL RSYYASWYQERPGQAPLLVIYGRNERPSGIPDRESASSSGNTASLTITGAQAEDEADYYCQVWDSFNEQVVFGGGTKLTV L II79 4QVQLVESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVHQA 17PGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCAKTYYGFWSGYYDYLGQGTLVTVS S GGGGSGGGGSGGGGSSSELTQDPAVSVGLGQTVTITCQG DSLRSYYANWYQQKPGQAPILVIYGENNRPSGIPDRFSGSSSGNTASLTITGAQAEDEADYYCHSRDSSGTHLRVFGGGT KLTVL II79 3QVQLLESGGGVVQPGTSLRLSCAASGFTESNYAINWVRQA 18AGKGLEWVSGISGSGVSTSYADSVKGRFTVSRDNSKNTLYLQMNSLRVEDTALYYCAKNGGGPEYLQHWGQGTLVTVSS G GGGSGGGGSGGGGSQSVLTQPPSASGTPGQRVTISCSGSS SNIGNNTVNWSRQLPGTAPKLLIYSNDQRPSGVPDRESGSKSGTSASLAITGLQPEDEADYYCGTWDSSLSAYVEGTGTK LTVL T5II-4B.1QVQLQESGGTLVQPGGSLRLSCAASGFTFSSYAMSWVRQA 19PGRGLEWVSTISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCAKGAYSGSYWGQGTLVTVSS GGGG SGGGGSGGGGSSSELTQDPAVSVALGQTVRITCQGDSLRS YYASWYQQKPGQAPSLVIYGENSRPSGIPDRESGSSSGNTASLTITGAQAENEADYYCQAWDSSTAVVEGGGTKLTVL T5II-4B.2QVQLQESGGTLVQPGGSLRLSCAASGFTESSYAMSWVRQA 20PGRGLEWVSTISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCAKGAYSGSHWGQGTLVTVSS GGGG SGGGGSGGGGSSSELTQDPAVSVALGQTVRITCQGDSLRS YYASWYQQKPGQAPSLVIYGENSRPSGIPDRESGSSSGNTASLTITGAQAENEADYYCQAWDSSTAVVFGGGTKLTVL RCI-11QVQLVESGAEVKKPGASVKVSCKASGYTFTSYGISWVRQA 21PGQGLEWMGWISAYNGNTNYAQKLQGRVTMTTDTSTSTAYMELRSLRSDDTAVYYCARPIYDSSGYDAFDIWGQGTMVTV SS GGGGSGGGGSGGGGSDIVMTQSPSTLSASIGDRVTITC RASEGIYHWLAWYQQKPGKAPKLLIYKASSLASGAPSRESGSGSGTDFTLTISSLQPDDFATYYCQQYHTISRTFGPGTK VDIK RCI-20QVQLVESGGGLVKPGGSLRLSCAASGFTESSYAMHWVRQA 22PGKGLEWVAVISYDGSNKYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYFCVRPSDSGWSFEHWGQGTLVPVSS G GGGSGGGGSGGGGSQSVLTQPPSASGTPGQRVTISCSGSS SNIGNNTVNWSRQLPGTAPKLLIYSNDQRPSGVPDRESGSKSGTSASLAITGLQPEDEADYYCGTWDSSLSAYVFGTGTK LTVL CI-11AQVQLQESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQA 23PGKGLEWVAVISYDGSNKYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCVRGDRSYGAEYFQHWGQGTLVTVS SGGGGSGGGGSGGGGSSSELTQDPAVSVASGQTVRITCQG DSLRSYYASWYQQKPGQAPLLVIYGKNIRPSGIPDRESGSTSGNSASLTITGAQAEDEADYYCNSRDSSGNRNWVEGGGT KLTVL CI-14AQVQLQESGGGLVKPGGSLRLSCAASGFTSSSYAMHWVRQA 24PGKGLEYVSAIGGNGGTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCAKEGEQWLEYRYYYGMDVWGQGTTV TVSSGGGGSGGGGSGGGGSSSELTQDPAVSVALGQTVRIT CQGDSLRSYYASWYQQKPGQAPSLVIYGENSRPSGIPDRESGSSSGNTASLTITGAQAENEADYYCQAWDSSTAVVEGGG TKLTVL S95-2QVQLVESGGGVVQPGRSLRLSCTASGFTESSYGMHWVRQA 25PGKGLEWVAVISYDGSNKYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARGGRYSSNWFSYYYYGMDVWGQG TTVTVSS GGGGSGGGGSGGGGSNEMLTQPPSVSVAPGKTA RITCGGNNIGSKSVYWYQQKPGQAPVLVVYDDSDRPSGIPERFSGSNSGNTATLTISRVEAGDEADYYCQVWDSSSDHVV FGGGTKVTVL

A) Chemical Synthesis.

Using the sequence information provided herein, the prostate cancerspecific antibodies of this invention (e.g., 3051.1, G12FC3, M6c42b,4F3YW, M40pr146, UA20, UA8, 585II41, 585II41.1, 585II56, 3076, 3051,M49R, RCI-14, I179_4, I179_3, T5II-4B.1, T5II-4B.2, RCI-11, RCI-20,CI-11A, CI-14A, S95-2, etc.), or variants thereof, can be chemicallysynthesized using well known methods of peptide synthesis. Solid phasesynthesis in which the C-terminal amino acid of the sequence is attachedto an insoluble support followed by sequential addition of the remainingamino acids in the sequence is one preferred method for the chemicalsynthesis of single chain antibodies. Techniques for solid phasesynthesis are described by Barany and Merrifield, Solid Phase PeptideSynthesis; pp. 3-284 in The Peptides: Analysis, Synthesis, Biology. Vol.2: Special Methods in Peptide Synthesis, Part A., Merrifield et al.(1963) J Am. Chem. Soc., 85: 2149-2156, and Stewart et al. (1984) SolidPhase Peptide Synthesis, 2nd ed. Pierce Chem. Co., Rockford, Ill.

B) Recombinant Expression of Prostate Cancer-Specific Antibodies.

In certain preferred embodiments, the prostate cancer specificantibodies of this invention (e.g., 3051.1, G12FC3, M6c42b, 4F3YW,M40pr146, UA20, UA8, 585II41, 585II41.1, 585II56, 3076, 3051, M49R,RCI-14, I179_4, I179_3, T5II-4B.1, T5II-4B.2, RCI-11, RCI-20, CI-11A,CI-14A, S95-2, etc.), or variants thereof, are prepared using standardtechniques well known to those of skill in the art. Using the sequenceinformation provided herein, nucleic acids encoding the desired antibodycan be chemically synthesized according to a number of standard methodsknown to those of skill in the art. Oligonucleotide synthesis, ispreferably carried out on commercially available solid phaseoligonucleotide synthesis machines (Needham-VanDevanter et al. (1984)Nucleic Acids Res. 12: 6159-6168) or manually synthesized using thesolid phase phosphoramidite triester method described by Beaucage et.al. (Beaucage et. al. (1981) Tetrahedron Letts. 22(20): 1859-1862).Alternatively, nucleic acids encoding the antibody can be amplifiedand/or cloned according to standard methods.

Molecular cloning techniques to achieve these ends are known in the art.A wide variety of cloning and in vitro amplification methods aresuitable for the construction of recombinant nucleic acids. Examples ofthese techniques and instructions sufficient to direct persons of skillthrough many cloning exercises are found in Berger and Kimmel, Guide toMolecular Cloning Techniques, Methods in Enzymology volume 152 AcademicPress, Inc., San Diego, CA (Berger); Sambrook et al. (1989) MolecularCloning—A Laboratory Manual (2nd ed.) Vol. 1-3, Cold Spring HarborLaboratory, Cold Spring Harbor Press, NY, (Sambrook); and CurrentProtocols in Molecular Biology, F. M. Ausubel et al., eds., CurrentProtocols, a joint venture between Greene Publishing Associates, Inc.and John Wiley & Sons, Inc., (1994 Supplement) (Ausubel). Methods ofproducing recombinant immunoglobulins are also known in the art. See,Cabilly, U.S. Pat. No. 4,816,567; and Queen et al. (1989) Proc. NatlAcad. Sci. USA 86: 10029-10033. In addition, detailed protocols for theexpression of antibodies are also provided by Liu et al. (2004) CancerRes. 64: 704-710, Poul et al. (2000) J Mol. Biol. 301: 1149-1161, andthe like.

C) Identification of Other Antibodies Binding the Same Epitope(s) asAntibodies 3051.1, G12FC3, M6c42b, 4F3YW, M40pr146, UA20, UA8, 585II41,585II41.1, 585II56, 3076, 3051, M49R, RCI-14, I179_4, I179_3, T5II-4B.1,T5II-4B.2, RCI-11, RCI-20, CI-11A, CI-14A, and/or S95-2.

Having identified useful prostate cancer specific internalizingantibodies (e.g., 3051.1, G12FC3, M6c42b, 4F3YW, M40pr146, UA20, UA8,585II41, 585II41.1, 585II56, 3076, 3051, M49R, RCI-14, I179_4, 11793,T5II-4B.1, T5II-4B.2, RCI-11, RCI-20, CI-11A, CI-14A, S95-2), other“related” internalizing prostate cancer specific antibodies can beidentified by screening for antibodies that cross-react with theidentified antibodies, either at the epitope bound by the antibodies,and/or for antibodies that cross-react with the identified antibodiesfor binding to a prostate cancer cell (e.g., CaP cells, PC3 cells,etc.), and/or with an idiotypic antibody raised against 3051.1, G12FC3,M6c42b, 4F3YW, M40pr146, UA20, UA8, 585II41, 585II41.1, 585II56, 3076,3051, M49R, RCI-14, I179_4, I179_3, T5II-4B.1, T5II-4B.2, RCI-11,RCI-20, CI-11A, CI-14A, and/or S95-2 antibodies of this invention.

1) Cross-Reactivity with Anti-Idiotypic Antibodies.

The idiotype represents the highly variable antigen-binding site of anantibody and is itself immunogenic. During the generation of anantibody-mediated immune response, an individual will develop antibodiesto the antigen as well as anti-idiotype antibodies, whose immunogenicbinding site (idiotype) mimics the antigen.

Anti-idiotypic antibodies can be raised against the variable regions ofthe antibodies identified herein using standard methods well known tothose of skill in the art. Briefly, anti-idiotype antibodies can be madeby injecting the antibodies of this invention, or fragments thereof(e.g., CDRs) into an animal thereby eliciting antisera against variousantigenic determinants on the antibody, including determinants in theidiotypic region.

Methods for the production of anti-analyte antibodies are well known inthe art. Large molecular weight antigens (greater than approx. 5000Daltons) can be injected directly into animals, whereas small molecularweight compounds (less than approx. 5000 Daltons) are preferably coupledto a high molecular weight immunogenic carrier, usually a protein, torender them immunogenic. The antibodies produced in response toimmunization can be utilized as serum, ascites fluid, an immunoglobulin(Ig) fraction, an IgG fraction, or as affinity-purified monospecificmaterial.

Polyclonal anti-idiotype antibodies can be prepared by immunizing ananimal with the antibodies of this invention prepared as describedabove. In general, it is desirable to immunize an animal which isspecies and allotype-matched with the animal from which the antibody(e.g. phage-display library) was derived. This minimizes the productionof antibodies directed against non-idiotypic determinants. The antiserumso obtained is then usually absorbed extensively against normal serumfrom the same species from which the phage-display library was derived,thereby eliminating antibodies directed against non-idiotypicdeterminants. Absorption can be accomplished by passing antiserum over agel formed by crosslinking normal (nonimmune) serum proteins withglutaraldehyde. Antibodies with anti-idiotypic specificity will passdirectly through the gel, while those having specificity fornon-idiotypic determinants will bind to the gel. Immobilizing nonimmuneserum proteins on an insoluble polysaccharide support (e.g., sepharose)also provides a suitable matrix for absorption.

Monoclonal anti-idiotype antibodies can be produced using the method ofKohler et al. (1975) Nature 256: 495. In particular, monoclonalanti-idiotype antibodies can be prepared using hybridoma technologywhich comprises fusing (1) spleen cells from a mouse immunized with theantigen or hapten-carrier conjugate of interest (i.e., the antibodies orthis invention or subsequences thereof) to (2) a mouse myeloma cell linewhich has been selected for resistance to a drug (e.g., 8-azaguanine).In general, it is desirable to use a myeloma cell line which does notsecrete an immunoglobulin. Several such lines are known in the art. Onegenerally preferred cell line is P3X63Ag8.653. This cell line is ondeposit at the American Type Culture Collection as CRL-1580.

Fusion can be carried out in the presence of polyethylene glycolaccording to established methods (see, e.g., Monoclonal Antibodies, R.Kennett, J. McKearn & K. Bechtol, eds. N.Y., Plenum Press, 1980, andCurrent Topics in Microbiology & Immunology, Vol. 81, F. Melchers, M.Potter & N. L. Warner, eds., N.Y., Springer-Verlag, 1978). The resultantmixture of fused and unfused cells is plated out inhypoxanthine-aminopterin-thymidine (HAT) selective medium. Under theseconditions, only hybrid cells will grow.

When sufficient cell growth has occurred, (typically 10⁻¹⁴ dayspost-fusion), the culture medium is harvested and screened for thepresence of monoclonal idiotypic, anti-analyte antibody by any one of anumber of methods which include solid phase RIA and enzyme-linkedimmunosorbent assay. Cells from culture wells containing antibody of thedesired specificity are then expanded and recloned. Cells from thosecultures that remain positive for the antibody of interest are thenusually passed as ascites tumors in susceptible, histocompatible,pristane-primed mice.

Ascites fluid is harvested by tapping the peritoneal cavity, retestedfor antibody, and purified as described above. If a nonsecreting myelomaline is used in the fusion, affinity purification of the monoclonalantibody is not usually necessary since the antibody is alreadyhomogeneous with respect to its antigen-binding characteristics. Allthat is necessary is to isolate it from contaminating proteins inascites, i.e., to produce an immunoglobulin fraction.

Alternatively, the hybrid cell lines of interest can be grown inserum-free tissue culture and the antibody harvested from the culturemedium. In general, this is a less desirable method of obtaining largequantities of antibody because the yield is low. It is also possible topass the cells intravenously in mice and to harvest the antibody fromserum. This method is generally not preferred because of the smallquantity of serum which can be obtained per bleed and because of theneed for extensive purification from other serum components. However,some hybridomas will not grow as ascites tumors and therefore one ofthese alternative methods of obtaining antibody must be used.

2) Cross-Reactivity with the 3051.1, G12FC3, M6c42b, 4F3YW, M40pr146,UA20, UA8, 585II41, 585II41.1, 585II56, 3076, 3051, M49R, RCI-14,I179_4, I179_3, T5II-4B.1, T5II-4B.2, RCI-11, RCI-20, CI-11A, CI-14A,and/or S95-2 antibodies of this invention.

In another approach, other prostate cancer specific antibodies of thisinvention can be identified by the fact that they bind the same epitopeas the “prototypic” antibodies of this invention (e.g 3051.1, G12FC3,M6c42b, 4F3YW, M40pr146, UA20, UA8, 585II41, 585II41.1, 585II56, 3076,3051, M49R, RCI-14, I179_4, I179_3, T5II-4B.1, T5II-4B.2, RCI-11,RCI-20, CI-11A, CI-14A, S95-2, etc.). To identify such antibodies, it snot necessary to isolate the subject epitope. In certain embodiments,one can screen, e.g. antibody libraries for antibodies that compete withthe prototypic antibodies of this invention for binding and/orinternalization by a prostate cancer cell (e.g. a CaP cell, a PC3 cell,etc.).

Methods of screening libraries for cell binding and/or internalizationare described in detail in the examples. Such screening methods, done,for example in the presence of labeled prototypic antibodies of thisinvention allows rapid identification of library members that competewith and exclude the prototypic antibodies of this invention frombinding and/or internalization into the target prostate cancer cell.

In addition, it is noted that methods of determining antibodycross-reactivity are well known to those of skill in the art. Generallythe epitope bound by the prototypic antibodies of this invention isdetermined e.g. by epitope mapping techniques. Methods of epitopemapping are well known to those of skill in the art (see, e.g., Reyes etal. (1992) Hepatitis E Virus (HEV): Epitope Mapping and Detection ofStrain Variation, Elsevier Science Publisher Shikata et al. eds.,Chapter 43:237-245; Li et al. (1993) Nature 363: 85-88). Epitope mappingcan be performed using Novatope system, a kit for which is commerciallyavailable from Novagen, Inc.

In certain embodiments, cross-reactive prostate cancer specificantibodies show at least 60%, preferably 80%, more preferably 90%, andmost preferably at least 95% or at least 99% cross-reactivity with oneor more of the prototypic antibodies of this invention.

D) Phage Display Methods to Select Other “Related” Prostate CancerSpecific Antibodies.

1) Chain Shuffling Methods.

One approach to creating modified single-chain antibody (scFv) generepertoires has been to replace the original V_(H) or V_(L) gene with arepertoire of V-genes to create new partners (chain shuffling) (Clacksonet al. (1991) Nature. 352: 624-628). Using chain shuffling and phagedisplay, the affinity of a human scFv antibody fragment that bound thehapten phenyloxazolone (phOx) was increased from 300 nM to 1 nM (300fold) (Marks et al. (1992) Bio/Technology 10: 779-783).

Thus, for example, to alter the affinity of a prostate cancer specificantibodies, a mutant scFv gene repertoire can be created containing aV_(H) gene of the prototypic antibodies (e.g. as shown in Tables 1-3,and/or FIGS. 7 and 8 ) antibody and a human V_(L) gene repertoire (lightchain shuffling). The scFv gene repertoire can be cloned into a phagedisplay vector, e.g., pHEN-1 (Hoogenboom et al. (1991) Nucleic AcidsRes., 19: 4133-4137) or other vectors, e.g. as described herein in theexamples, and after transformation a library of transformants isobtained.

Similarly, for heavy chain shuffling, the prostate cancer specificantibody (e.g., 3051.1, G12FC3, M6c42b, 4F3YW, M40pr146, UA20, UA8,585II41, 585II41.1, 585II56, 3076, 3051, M49R, RCI-14, I179_4, I179_3,T5II-4B.1, T5II-4B.2, RCI-11, RCI-20, CI-11A, CI-14A, S95-2, etc.) V_(H)CDR1 and/or CDR2, and/or CDR3 and light chain (see, e.g., Table 2) arecloned into a vector containing a human V_(H) gene repertoire to createa phage antibody library transformants. For detailed descriptions ofchain shuffling to increase antibody affinity see Schier et al. (1996)J. Mol. Biol., 255: 28-43, and the like.

2) Site-Directed Mutagenesis to Improve Binding Affinity.

The majority of antigen contacting amino acid side chains are typicallylocated in the complementarity determining regions (CDRs), three in theV_(H) (CDR1, CDR2, and CDR3) and three in the V_(L) (CDR1, CDR2, andCDR3) (Chothia et al. (1987) J Mol. Biol., 196: 901-917; Chothia et al.(1986) Science, 233: 755-8; Nhan et al. (1991) J Mol. Biol., 217:133-151). These residues contribute the majority of binding energeticsresponsible for antibody affinity for antigen. In other molecules,mutating amino acids which contact ligand has been shown to be aneffective means of increasing the affinity of one protein molecule forits binding partner (Lowman et al. (1993) J. Mol. Biol., 234: 564-578;Wells (1990) Biochemistry, 29: 8509-8516). Site-directed mutagenesis ofCDRs and screening against the prostate cancer cells, e.g. as describedherein in the examples, can produce antibodies having improved bindingaffinity.

3) CDR Randomization to Produce Higher Affinity Human scFv.

In an extension of simple site-directed mutagenesis, mutant antibodylibraries can be created where partial or entire CDRs are randomized(V_(L) CDR1 CDR2 and/or CDR3 and/or V_(H) CDR1, CDR2 and/or CDR3). Inone embodiment, each CDR is randomized in a separate library, using aknown antibody (e.g., 3051.1, G12FC3, M6c42b, 4F3YW, M40pr146, UA20,UA8, 585II41, 585II41.1, 585II56, 3076, 3051, M49R, RCI-14, 1179_4,I179_3, T5II-4B.1, T5II-4B.2, RCI-11, RCI-20, CI-11A, CI-14A, and/orS95-2) as a template. The CDR sequences of the highest affinity mutantsfrom each CDR library are combined to obtain an additive increase inaffinity. A similar approach has been used to increase the affinity ofhuman growth hormone (hGH) for the growth hormone receptor over 1500fold from 3.4×10⁻¹⁰ to 9.0×10⁻¹³ M (Lowman et al. (1993) J. Mol. Biol.,234: 564-578).

V_(H) CDR3 often occupies the center of the binding pocket, and thusmutations in this region are likely to result in an increase in affinity(Clackson et al. (1995) Science, 267: 383-386). In one embodiment, fourV_(H) CDR3 residues are randomized at a time using the nucleotides NNS(see, e.g., Schier et al. (1996) Gene, 169: 147-155; Schier and Marks(1996) Human Antibodies and Hybridomas. 7: 97-105, 1996; and Schier etal. (1996) J. Mol. Biol. 263: 551-567).

E) Creation of Other Antibody Forms.

Using the known and/or identified sequences (e.g. V_(H) and/or V_(L)sequences) of the single chain antibodies provided herein other antibodyforms can readily be created. Such forms include, but are not limited tomultivalent antibodies, full antibodies, scFv, (scFv′)₂, Fab, (Fab′)₂,chimeric antibodies, and the like.

1) Creation of Homodimers.

For example, to create (scFv′)₂ antibodies, two prostate cancer specificscFvs are joined, either through a linker (e.g., a carbon linker, apeptide, etc.) or through a disulfide bond between, for example, twocysteins. Thus, for example, to create disulfide linked scFv, a cysteineresidue can be introduced by site directed mutagenesis at thecarboxy-terminus of the antibodies described herein.

An scFv can be expressed from this construct, purified by IMAC, andanalyzed by gel filtration. To produce (scFv′)₂ dimers, the cysteine isreduced by incubation with 1 mM 3-mercaptoethanol, and half of the scFvblocked by the addition of DTNB. Blocked and unblocked scFvs areincubated together to form (scFv′)₂ and the resulting material can beanalyzed by gel filtration. The affinity of the resulting dimmer can bedetermined using standard methods, e.g. by BIAcore.

In one particularly preferred embodiment, the (scFv′)₂ dimer is createdby joining the scFv′ fragments through a linker, more preferably througha peptide linker. This can be accomplished by a wide variety of meanswell known to those of skill in the art. For example, one preferredapproach is described by Holliger et al. (1993) Proc. Natl. Acad. Sci.USA, 90: 6444-6448 (see also WO 94/13804).

It is noted that using the V_(H) and/or V_(L) sequences provided hereinFabs and (Fab′)₂ dimers can also readily be prepared. Fab is a lightchain joined to V_(H)-C_(H)1 by a disulfide bond and can readily becreated using standard methods known to those of skill in the art. TheF(ab)′₂ can be produced by dimerizing the Fab, e.g. as described abovefor the (scFv′)₂ dimer.

2) Chimeric Antibodies.

The antibodies of this invention also include “chimeric” antibodies inwhich a portion of the heavy and/or light chain is identical with orhomologous to corresponding sequences in antibodies derived from aparticular species or belonging to a particular antibody class orsubclass, while the remainder of the chain(s) is identical with orhomologous to corresponding sequences in antibodies derived from anotherspecies or belonging to another antibody class or subclass, as well asfragments of such antibodies, so long as they exhibit the desiredbiological activity (see, e.g., U.S. Pat. No. 4,816,567; Morrison et al.(1984) Proc. Natl. Acad. Sci. 81: 6851-6855, etc.).

While the prototypic antibodies provided herein are fully humanantibodies, chimeric antibodies are contemplated, particularly when suchantibodies are to be used in species other than humans (e.g., inveterinary applications). Chimeric antibodies are antibodies comprisinga portions from two different species (e.g. a human and non-humanportion). Typically, the antigen combining region (or variable region)of a chimeric antibody is derived from a one species source and theconstant region of the chimeric antibody (which confers biologicaleffector function to the immunoglobulin) is derived from another source.A large number of methods of generating chimeric antibodies are wellknown to those of skill in the art (see, e.g., U.S. Pat. Nos. 5,502,167,5,500,362, 5,491,088, 5,482,856, 5,472,693, 5,354,847, 5,292,867,5,231,026, 5,204,244, 5,202,238, 5,169,939, 5,081,235, 5,075,431, and4,975,369, and PCT application WO 91/0996).

In general, the procedures used to produce chimeric antibodies consistof the following steps (the order of some steps may be interchanged):(a) identifying and cloning the correct gene segment encoding theantigen binding portion of the antibody molecule; this gene segment(known as the VDJ, variable, diversity and joining regions for heavychains or VJ, variable, joining regions for light chains, or simply asthe V or variable region or V_(H) and V_(L) regions) may be in eitherthe cDNA or genomic form; (b) cloning the gene segments encoding thehuman constant region or desired part thereof; (c) ligating the variableregion to the constant region so that the complete chimeric antibody isencoded in a transcribable and translatable form; (d) ligating thisconstruct into a vector containing a selectable marker and gene controlregions such as promoters, enhancers and poly(A) addition signals; (e)amplifying this construct in a host cell (e.g., bacteria); (f)introducing the DNA into eukaryotic cells (transfection) most oftenmammalian lymphocytes; and culturing the host cell under conditionssuitable for expression of the chimeric antibody.

Antibodies of several distinct antigen binding specificities have beenmanipulated by these protocols to produce chimeric proteins (e.g.,anti-TNP: Boulianne et al. (1984) Nature, 312: 643; and anti-tumorantigens: Sahagan et al. (1986) J. Immunol., 137: 1066). Likewiseseveral different effector functions have been achieved by linking newsequences to those encoding the antigen binding region. Some of theseinclude enzymes (Neuberger et al. (1984) Nature 312: 604),immunoglobulin constant regions from another species and constantregions of another immunoglobulin chain (Sharon et al. (1984) Nature309: 364; Tan et al., (1985) J Immunol. 135: 3565-3567).

In certain embodiments, a recombinant DNA vector is used to transfect acell line that produces a prostate cancer specific antibody of thisinvention. The novel recombinant DNA vector contains a “replacementgene” to replace all or a portion of the gene encoding theimmunoglobulin constant region in the cell line (e.g., a replacementgene may encode all or a portion of a constant region of a humanimmunoglobulin, a specific immunoglobulin class, or an enzyme, a toxin,a biologically active peptide, a growth factor, inhibitor, or a linkerpeptide to facilitate conjugation to a drug, toxin, or other molecule,etc.), and a “target sequence” that allows for targeted homologousrecombination with immunoglobulin sequences within the antibodyproducing cell.

In another embodiment, a recombinant DNA vector is used to transfect acell line that produces an antibody having a desired effector function,(e.g., a constant region of a human immunoglobulin) in which case, thereplacement gene contained in the recombinant vector may encode all or aportion of a region of a prostate cancer specific antibody of thisinvention and the target sequence contained in the recombinant vectorallows for homologous recombination and targeted gene modificationwithin the antibody producing cell. In either embodiment, when only aportion of the variable or constant region is replaced, the resultingchimeric antibody can define the same antigen and/or have the sameeffector function yet be altered or improved so that the chimericantibody may demonstrate a greater antigen specificity, greater affinitybinding constant, increased effector function, or increased secretionand production by the transfected antibody producing cell line, etc.

Regardless of the embodiment practiced, the processes of selection forintegrated DNA (via a selectable marker), screening for chimericantibody production, and cell cloning, can be used to obtain a clone ofcells producing the chimeric antibody.

Thus, a piece of DNA that encodes a modification for a monoclonalantibody can be targeted directly to the site of the expressedimmunoglobulin gene within a B-cell or hybridoma cell line. DNAconstructs for any particular modification can be made to alter theprotein product of any monoclonal cell line or hybridoma. The level ofexpression of chimeric antibody should be higher when the gene is at itsnatural chromosomal location rather than at a random position. Detailedmethods for preparation of chimeric (humanized) antibodies can be foundin U.S. Pat. No. 5,482,856.

3) Intact Human Antibodies.

In another embodiment, this invention provides for intact, fully humanprostate cancer specific antibodies. Such antibodies can readily beproduced in a manner analogous to making chimeric human antibodies. Inthis instance, instead of using a recognition function derived, e.g.from a murine, the fully human recognition function (e.g., V_(H) andV_(L)) of the antibodies described herein is utilized.

4) Diabodies.

In certain embodiments, this invention contemplates diabodies comprisingone or more of the V_(H) and V_(L) domains described herein. The term“diabodies” refers to antibody fragments typically having twoantigen-binding sites. The fragments typically comprise a heavy chainvariable domain (V_(H)) connected to a light chain variable domain(V_(L)) in the same polypeptide chain (V_(H)-V_(L)). By using a linkerthat is too short to allow pairing between the two domains on the samechain, the domains are forced to pair with the complementary domains ofanother chain and create two antigen-binding sites. Diabodies aredescribed more fully in, for example, EP 404,097; WO 93/11161, andHolliger et al. (1993) Proc. Natl. Acad. Sci. USA 90: 6444-6448.

5) Unibodies.

In certain embodiments using the sequence information provided herein,the antibodies of this invention can be constructed as unibodies.UniBody are antibody technology that produces a stable, smaller antibodyformat with an anticipated longer therapeutic window than certain smallantibody formats. In certain embodiments unibodies are produced fromIgG4 antibodies by eliminating the hinge region of the antibody. Unlikethe full size IgG4 antibody, the half molecule fragment is very stableand is termed a uniBody. Halving the IgG4 molecule leaves only one areaon the UniBody that can bind to a target. Methods of producing unibodiesare described in detail in PCT Publication WO2007/059782, which isincorporated herein by reference in its entirety (see, also, Kolfschotenet al. (2007) Science 317: 1554-1557).

6) Affibodies.

In certain embodiments the sequence information provided herein is usedto construct affibody molecules that bind prostate cancer cells.Affibody molecules are class of affinity proteins based on a 58-aminoacid residue protein domain, derived from one of the IgG-binding domainsof staphylococcal protein A. This three helix bundle domain has beenused as a scaffold for the construction of combinatorial phagemidlibraries, from which affibody variants that target the desiredmolecules can be selected using phage display technology (see, e.g,.Nord et al. (1997) Nat. Biotechnol. 15: 772-777; Ronmark et al. (2002)Eur. J. Biochem., 269: 2647-2655.). Details of Affibodies and methods ofproduction are known to those of skill (see, e.g., U.S. Pat. No.5,831,012 which is incorporated herein by reference in its entirety).

It will be recognized that the antibodies described above can beprovided as whole intact antibodies (e.g., IgG), antibody fragments, orsingle chain antibodies, using methods well known to those of skill inthe art. In addition, while the antibody can be from essentially anymammalian species, to reduce immunogenicity, it is desirable to use anantibody that is of the species in which the antibody and/or chimericmoiety is to be used. In other words, for use in a human, it isdesirable to use a human, humanized, or chimeric human antibody.

7) Measurement of Antibody/Polypeptide Binding Affinity

As explained above, selection for increased avidity can involvesmeasuring the affinity of the antibody for the target antigen (e.g., aprostate cancer cell). Methods of making such measurements are wellknown to those of skill in the art. Briefly, for example, the K_(d) ofthe antibody is determined from the kinetics of binding to, e.g. thetarget cell in a BIAcore, a biosensor based on surface plasmonresonance. For this technique, the antigen or cell is coupled to aderivatized sensor chip capable of detecting changes in mass. Whenantibody is passed over the sensor chip, antibody binds to the antigenresulting in an increase in mass that is quantifiable. Measurement ofthe rate of association as a function of antibody concentration can beused to calculate the association rate constant (k_(on)). After theassociation phase, buffer is passed over the chip and the rate ofdissociation of antibody (k_(off)) determined. K_(on) is typicallymeasured in the range 1.0×10² to 5.0×10⁶ and k_(off) in the range1.0×10⁻¹ to 1.0×10⁻⁶. The equilibrium constant K_(d) is often calculatedas k_(off)/k_(on) and thus is typically measured in the range 10⁻⁵ to10⁻¹². Affinities measured in this manner correlate well with affinitiesmeasured in solution by fluorescence quench titration.

III. Chimeric Moieties Comprisin2 Anti-Prostate Cancer Antibodies.

The prototypical prostate cancer-specific antibodies of this invention(e.g., 3051.1, G12FC3, M6c42b, 4F3YW, M40pr146, UA20, UA8, 585II41,585II41.1, 585II56, 3076, 3051, M49R, RCI-14, I179_4, I179_3, T5II-4B.1,T5II-4B.2, RCI-11, RCI-20, CI-11A, CI-14A, S95-2, etc.) specificallybind to and are internalized by prostate cancer cells. The antibodiescan be used alone as therapeutics (e.g. to inhibit growth and/orproliferation of a prostate cancer cell) or they can be coupled to aneffector to provide efficient and specific delivery of the effector(e.g. an effector molecule such as a cytotoxin, a radiolabel, a cancerdrug, etc.) to various prostate cancer cells (e.g. isolated cells,metastatic cells, solid tumor cells, etc.).

In certain preferred embodiments, the antibodies of this invention areutilized in a “pretargeting” strategy (resulting in formation of achimeric moiety at the target site after administration of the effectormoiety) or in a “targeting” strategy where the antibody is coupled to aneffector molecule prior to use to provide a chimeric molecule.

A chimeric molecule or chimeric composition or chimeric moiety refers toa molecule or composition wherein two or more molecules that existseparately in their native state are joined together to form a singlemolecule having the desired functionality of its constituent molecules.Typically, one of the constituent molecules of a chimeric molecule is a“targeting molecule. The targeting molecule is a molecule such as aligand or an antibody that specifically binds (and, in certainembodiments, is internalized) by its corresponding target, e.g., aprostate cancer cell.

Another constituent of the chimeric moiety is an “effector”. Theeffector refers to a molecule or group of molecules that is to bespecifically/preferentially transported to or into the target cell(e.g., a prostate cancer cell). It is noted that in this context, suchspecific transport need not be exclusively to or into a cancer cell, butmerely need to provide preferential delivery of the effector to or intothe cancer cell as compared to normal healthy cells.

The effector molecule typically has a characteristic activity that is tobe delivered to or into the target cell. Effector molecules include, butare not limited to cytotoxins, labels, radionuclides, ligands,antibodies, drugs, liposomes, nanoparticles, viral particles, cytokines,and the like.

In certain embodiments, the effector comprises a detectable label.Suitable detectable labels include, but are not limited to radio-opaquelabels, nanoparticles, PET labels, MRI labels, radioactive labels, andthe like. Among the radionuclides and useful in various embodiments ofthe present invention, gamma-emitters, positron-emitters, x-ray emittersand fluorescence-emitters are suitable for localization, diagnosisand/or staging, and/or therapy, while beta and alpha-emitters andelectron and neutron-capturing agents, such as boron and uranium, alsocan be used for therapy.

The detectable labels can be used in conjunction with an externaldetector and/or an internal detector and provide a means of effectivelylocalizing and/or visualizing prostate cancer cells. Suchdetection/visualization can be useful in various contexts including, butnot limited to pre-operative and intraoperative settings. Thus, incertain embodiment this invention relates to a method ofintraoperatively detecting and prostate cancers in the body of a mammal.These methods typically involve administering to the mammal acomposition comprising, in a quantity sufficient for detection by adetector (e.g. a gamma detecting probe), an prostate cancer specificantibody labeled with a detectable label (e.g. antibodies of thisinvention labeled with a radioisotope, e.g. ¹⁶¹Tb, ¹²³I, ¹²⁵I, and thelike), and, after allowing the active substance to be taken up by thetarget tissue, and preferably after blood clearance of the label,subjecting the mammal to a radioimmunodetection technique in therelevant area of the body, e.g. by using a gamma detecting probe.

In certain embodiments the label-bound antibody can be used in thetechnique of radioguided surgery, wherein relevant tissues in the bodyof a subject can be detected and located intraoperatively by means of adetector, e.g. a gamma detecting probe. The surgeon can,intraoperatively, use this probe to find the tissues in which uptake ofthe compound labeled with a radioisotope, that is, e.g. a low-energygamma photon emitter, has taken place. In certain embodiments suchmethods are particularly useful in localizing and removing secondarycancers produced by metastatic cells from a primary tumor.

In addition to detectable labels, certain preferred effectors include,but are not limited to cytotoxins (e.g. Pseudomonas exotoxin, ricin,abrin, Diphtheria toxin, and the like), or cytotoxic drugs or prodrugs,in which case the chimeric molecule may act as a potent cell-killingagent specifically targeting the cytotoxin to prostate cancer cells.

In still other embodiments, the effector can include a liposomeencapsulating a drug (e.g. an anti-cancer drug such as abraxane,doxorubicin, pamidronate disodium, anastrozole, exemestane,cyclophosphamide, epirubicin, toremifene, letrozole, trastuzumab,megestroltamoxifen, paclitaxel, docetaxel, capecitabine, goserelinacetate, zoledronic acid, vinblastine, etc.), an antigen that stimulatesrecognition of the bound cell by components of the immune system, anantibody that specifically binds immune system components and directsthem to the prostate cancer, and the like.

A) Illustrative Effectors.

1) Imaging Compositions.

In certain embodiments, the chimeric moieties of this invention can beused to direct detectable labels to a tumor site. This can facilitatetumor detection and/or localization. It can be effective for detectingprimary tumors, or, in certain embodiments, secondary tumors producedby, e.g., prostate metastatic cells. In certain embodiments, theeffector component of the chimeric moiety comprises a “radio-opaque”label, e.g. a label that can be easily visualized using x-rays.Radio-opaque materials are well known to those of skill in the art. Themost common radio-opaque materials include iodide, bromide or bariumsalts. Other radiopaque materials are also known and include, but arenot limited to, organic bismuth derivatives (see, e.g., U.S. Pat. No.5,939,045), radio-opaque polyurethanes (see, e.g., U.S. Pat. No.5,346,981), organobismuth composites (see, e.g., U.S. Pat. No.5,256,334), radio-opaque barium polymer complexes (see, e.g., U.S. Pat.No. 4,866,132), and the like.

The antibodies of this invention can be coupled directly to theradio-opaque moiety or they can be attached to a “package” (e.g., achelate, a liposome, a polymer microbead, a nanoparticle, etc.)carrying, containing, or comprising the radio-opaque material, e.g., asdescribed below.

In addition to radio-opaque labels, other labels are also suitable foruse in this invention. Detectable labels suitable for use as theeffector molecule component of the chimeric moietys of this inventioninclude any composition detectable by spectroscopic, photochemical,biochemical, immunochemical, electrical, optical or chemical means.Useful labels in the present invention include magnetic beads (e.g.,DYNABEADS™), fluorescent dyes (e.g., fluorescein isothiocyanate, texasred, rhodamine, green fluorescent protein, and the like), radiolabels(e.g., ³H, ¹²⁵I, ³⁵S, ¹⁴C, or ³²P), enzymes (e.g., horse radishperoxidase, alkaline phosphatase and others commonly used in an ELISA),and colorimetric labels such as colloidal gold or colored glass orplastic (e.g. polystyrene, polypropylene, latex, etc.) beads,nanoparticles, quantum dots, and the like.

In certain embodiments, suitable radiolabels include, but are notlimited to, ⁹⁹Tc, ²⁰³Pb, ⁶⁷Ga, ⁶⁸Ga, ⁷²As, ¹¹¹In, ^(113m)In, ⁹⁷Ru, ⁶²Cu,641Cu, ⁵²Fe, ^(52m)Mn, ⁵¹Cr, ¹⁸⁶Re, ¹⁸⁸Re, ⁷⁷As, ⁹⁰Y, ⁶⁷Cu, ¹⁶⁹Er, ¹²Sn,¹²⁷Te, ¹⁴²Pr, ¹⁴³Pr, ¹⁹⁸Au, ¹⁹⁹Au, ¹⁶¹Tb, ¹⁰⁹Pd, ¹⁶⁵Dy, ¹⁴⁹Pm, ¹⁵¹Pm,¹⁵³Sm, ¹⁵⁷Gd ¹⁵⁹Gd, ¹⁶⁶Ho, ¹⁷²Tm, ¹⁶⁹Yb, ¹⁷⁵Yb, ¹⁷⁷Lu, ¹⁰⁵Rh, and ¹¹¹Ag.

Means of detecting such labels are well known to those of skill in theart. Thus, for example, certain radiolabels may be detected usingphotographic film, scintillation detectors, PET imaging, MRI, and thelike. Fluorescent markers can be detected using a photodetector todetect emitted illumination. Enzymatic labels are typically detected byproviding the enzyme with a substrate and detecting the reaction productproduced by the action of the enzyme on the substrate, and colorimetriclabels are detected by simply visualizing the colored label.

2) Radiosensitizers.

In another embodiment, the effector can comprise a radiosensitizer thatenhances the cytotoxic effect of ionizing radiation (e.g., such as mightbe produced by ⁶⁰Co or an x-ray source) on a cell. Numerousradiosensitizing agents are known and include, but are not limited tobenzoporphyrin derivative compounds (see, e.g., U.S. Pat. No.5,945,439), 1,2,4-benzotriazine oxides (see, e.g., U.S. Pat. No.5,849,738), compounds containing certain diamines (see, e.g., U.S. Pat.No. 5,700,825), BCNT (see, e.g., U.S. Pat. No. 5,872,107),radiosensitizing nitrobenzoic acid amide derivatives (see, e.g., U.S.Pat. No. 4,474,814), various heterocyclic derivatives (see, e.g., U.S.Pat. No. 5,064,849), platinum complexes (see, e.g., U.S. Pat. No.4,921,963), and the like.

3) Alpha Emitters.

In certain embodiments, the effector can include an alpha emitter, i.e.a radioactive isotope that emits alpha particles. Alpha-emitters haverecently been shown to be effective in the treatment of cancer (see,e.g., McDevitt et al. (2001) Science 294:1537-1540; Ballangrud et al.(2001) Cancer Res. 61: 2008-2014; Borchardt et al. (2003) Cancer Res.63: 5084-50). Suitable alpha emitters include, but are not limited toBi, ²¹³Bi, ²¹¹At, and the like.

4) Ligands.

The effector molecule can also comprise a ligand, an epitope tag, or anantibody. In certain embodiments preferred ligands and antibodiesinclude those that bind to surface markers on immune cells. Chimericmoietys utilizing such antibodies as effector molecules act asbifunctional linkers establishing an association between the immunecells bearing binding partner for the ligand or antibody and theprostate cancer cell(s).

5) Chelates

Many of the pharmaceuticals and/or radiolabels described herein can beprovided as a chelate, particularly where a pre-targeting strategy isutilized. The chelating molecule is typically coupled to a molecule(e.g. biotin, avidin, streptavidin, etc.) that specifically binds anepitope tag attached to a prostate cancer specific antibody of thisinvention.

Chelating groups are well known to those of skill in the art. In certainembodiments, chelating groups are derived from ethylene diaminetetra-acetic acid (EDTA), diethylene triamine penta-acetic acid (DTPA),cyclohexyl 1,2-diamine tetra-acetic acid (CDTA),ethyleneglycol-O,O′-bis(2-aminoethyl)-N,N,N′,N′-tetra-acetic acid(EGTA), N,N-bis(hydroxybenzyl)-ethylenediamine-N,N′-diacetic acid(HBED), triethylene tetramine hexa-acetic acid (TTHA),1,4,7,10-tetraazacyclododecane-N,N′-,N″,N″′-tetra-acetic acid (DOTA),hydroxyethyldiamine triacetic acid (HEDTA),1,4,8,11-tetra-azacyclotetradecane-N,N′,N″,N″′-tetra-acetic acid (TETA),substituted DTPA, substituted EDTA, and the like.

Examples of certain preferred chelators include unsubstituted or,substituted 2-iminothiolanes and 2-iminothiacyclohexanes, in particular2-imino-4-mercaptomethylthiolane.

One chelating agent, 1,4,7,10-tetraazacyclododecane-N, N, N″,N″′-tetraacetic acid (DOTA), is of particular interest because of itsability to chelate a number of diagnostically and therapeuticallyimportant metals, such as radionuclides and radiolabels.

Conjugates of DOTA and proteins such as antibodies have been described.For example, U.S. Pat. No. 5,428,156 teaches a method for conjugatingDOTA to antibodies and antibody fragments. To make these conjugates, onecarboxylic acid group of DOTA is converted to an active ester which canreact with an amine or sulfhydryl group on the antibody or antibodyfragment. Lewis et al. (1994) Bioconjugate Chem. 5: 565-576, describes asimilar method wherein one carboxyl group of DOTA is converted to anactive ester, and the activated DOTA is mixed with an antibody, linkingthe antibody to DOTA via the epsilon-amino group of a lysine residue ofthe antibody, thereby converting one carboxyl group of DOTA to an amidemoiety.

In certain embodiments the chelating agent can be coupled, directly orthrough a linker, to an epitope tag or to a moiety that binds an epitopetag. Conjugates of DOTA and biotin have been described (see, e.g., Su(1995) J Nucl. Med., 36 (5 Suppl):154P, which discloses the linkage ofDOTA to biotin via available amino side chain biotin derivatives such asDOTA-LC-biotin or DOTA-benzyl-4-(6-amino-caproamide)-biotin). Yau etal., WO 95/15335, disclose a method of producing nitro-benzyl-DOTAcompounds that can be conjugated to biotin. The method comprises acyclization reaction via transient projection of a hydroxy group;tosylation of an amine; deprotection of the transiently protectedhydroxy group; tosylation of the deprotected hydroxy group; andintramolecular tosylate cyclization. Wu et al. (1992) Nucl. Med. Biol.,19(2): 239-244 discloses a synthesis of macrocylic chelating agents forradiolabeling proteins with ¹¹¹IN and ⁹⁰Y. Wu et al. makes a labeledDOTA-biotin conjugate to study the stability and biodistribution ofconjugates with avidin, a model protein for studies. This conjugate wasmade using a biotin hydrazide which contained a free amino group toreact with an in situ generated activated DOTA derivative.

6) Cytotoxins.

The antibodies of this invention can be used to deliver a variety ofcytotoxic drugs including therapeutic drugs, a compound emittingradiation, molecules of plants, fungal, or bacterial origin, biologicalproteins, and mixtures thereof. The cytotoxic drugs can beintracellularly acting cytotoxic drugs, such as short-range radiationemitters, including, for example, short-range, high-energy α-emitters asdescribed above.

Enzymatically active toxins and fragments. thereof are exemplified bydiphtheria toxin A fragment, nonbinding active fragments of diphtheriatoxin, exotoxin A (from Pseudomonas aeruginosa), ricin A chain, abrin Achain, modeccin A chain, .alpha.-sacrin, certain Aleurites fordiiproteins, certain Dianthin proteins, Phytolacca americana proteins (PAP,PAPII and PAP-S), Morodica charantia inhibitor, curcin, crotin,Saponaria officinalis inhibitor, gelonin, mitogillin, restrictocin,phenomycin, and enomycin, for example.

In certain embodiments the cytotoxins can include, but are not limitedto Pseudomonas exotoxins, Diphtheria toxins, ricin, abrin andderivatives thereof. Pseudomonas exotoxin A (PE) is an extremely activemonomeric protein (molecular weight 66 kD), secreted by Pseudomonasaeruginosa, which inhibits protein synthesis in eukaryotic cells throughthe inactivation of elongation factor 2 (EF-2) by catalyzing itsADP-ribosylation (catalyzing the transfer of the ADP ribosyl moiety ofoxidized NAD onto EF-2).

The toxin contains three structural domains that act in concert to causecytotoxicity. Domain Ia (amino acids 1-252) mediates cell binding.Domain II (amino acids 253-364) is responsible for translocation intothe cytosol and domain III (amino acids 400-613) mediates ADPribosylation of elongation factor 2, which inactivates the protein andcauses cell death. The function of domain Ib (amino acids 365-399)remains undefined, although a large part of it, amino acids 365-380, canbe deleted without loss of cytotoxicity. See Siegall et al. (1989) JBiol. Chem. 264: 14256-14261.

In certain embodiments the antibody is attached to a preferred moleculein which domain Ia (amino acids 1 through 252) is deleted and aminoacids 365 to 380 have been deleted from domain Ib. In certainembodiments all of domain Ib and a portion of domain II (amino acids 350to 394) can be deleted, particularly if the deleted sequences arereplaced with a linking peptide.

In addition, the PE and other cytotoxic proteins can be further modifiedusing site-directed mutagenesis or other techniques known in the art, toalter the molecule for a particular desired application. For example,means to alter the PE molecule in a manner that does not substantiallyaffect the functional advantages provided by the PE molecules describedhere can also be used and such resulting molecules are intended to becovered herein.

Methods of cloning genes encoding PE fused to various ligands are wellknown to those of skill in the art (see, e.g., Siegall et al. (1989)FASEB J, 3: 2647-2652; and Chaudhary et al. (1987) Proc. Natl. Acad.Sci. USA, 84: 4538-4542).

Like PE, diphtheria toxin (DT) kills cells by ADP-ribosylatingelongation factor 2 thereby inhibiting protein synthesis. Diphtheriatoxin, however, is divided into two chains, A and B, linked by adisulfide bridge. In contrast to PE, chain B of DT, which is on thecarboxyl end, is responsible for receptor binding and chain A, which ispresent on the amino end, contains the enzymatic activity (Uchida et al.(1972) Science, 175: 901-903; Uchida et al. (1973) J Biol. Chem., 248:3838-3844).

In certain embodiments, the antibody-Diphtheria toxin chimeric moietysof this invention have the native receptor-binding domain removed bytruncation of the Diphtheria toxin B chain. One illustrative modifiedDiphtheria toxin is DT388, a DT in which the carboxyl terminal sequencebeginning at residue 389 is removed (see, e.g., Chaudhary et al. (1991)Bioch. Biophys. Res. Comm., 180: 545-551). Like the PE chimericcytotoxins, the DT molecules can be chemically conjugated to theprostate cancer specific antibody, but, in certain preferredembodiments, the antibody will be fused to the Diphtheria toxin byrecombinant means (see, e.g., Williams et al. (1990) J Biol. Chem. 265:11885-11889).

7) Viral Particles.

In certain embodiments, the effector comprises a viral particle (e.g., afilamentous phage, an adeno-associated virus (AAV), a lentivirus, andthe like). The antibody can be conjugated to the viral particle and/orcan be expressed on the surface of the viral particle (e.g. afilamentous phage). The viral particle can additionally include anucleic acid that is to be delivered to the target (e.g., prostatecancer) cell. The use of viral particles to deliver nucleic acids tocells is described in detail in WO 99/55720, U.S. Pat. Nos. 6,670,188,6,642,051, and 6,669,936.

8) Other Therapeutic Moieties.

Other suitable effector molecules include pharmacological agents orencapsulation systems containing various pharmacological agents. Thus,the targeting molecule of the chimeric moiety can be attached directlyto a drug that is to be delivered directly to the tumor. Such drugs arewell known to those of skill in the art and include, but are not limitedto, abraxane, doxorubicin, pamidronate disodium, anastrozole,exemestane, cyclophosphamide, epirubicin, toremifene, letrozole,trastuzumab, megestroltamoxifen, paclitaxel, docetaxel, capecitabine,goserelin acetate, zoledronic acid, vinblastine, etc.), an antisensemolecule, an SiRNA, and the like.

Alternatively, the effector molecule can comprise an encapsulationsystem, such as a viral capsid, a liposome, or micelle that contains atherapeutic composition such as a drug, a nucleic acid (e.g. anantisense nucleic acid or another nucleic acid to be delivered to thecell), or another therapeutic moiety that is preferably shielded fromdirect exposure to the circulatory system. Means of preparing liposomesattached to antibodies are well known to those of skill in the art. See,for example, U.S. Pat. No. 4,957,735, Connor et al. (1985) Pharm. Ther.,28: 341-365. In addition coupling of liposomes to antibodies of thisinvention is illustrated herein in the Examples.

B) Attachment of the Antibody to the Effector.

One of skill will appreciate that the antibodies of this invention andthe effector molecule(s) can be joined together in any order. Thus,where antibody is a single chain polypeptide, the effector molecule canbe joined to either the amino or carboxy termini of the targetingmolecule. The targeting molecule can also be joined to an internalregion of the effector molecule, or conversely, the effector moleculecan be joined to an internal location of the targeting molecule, as longas the attachment does not interfere with the respective activities ofthe molecules.

The antibody and the effector can be attached by any of a number ofmeans well known to those of skill in the art. Typically the effector isconjugated, either directly or through a linker (spacer), to thetargeting molecule. However, In certain embodiments, where both theeffector molecule and the antibody are polypeptides it is preferable torecombinantly express the chimeric molecule as a single-chain fusionprotein.

1) Conjugation of the Effector Molecule to the Antibody.

In one embodiment, the prostate cancer specific antibody is chemicallyconjugated to the effector molecule (e.g., a cytotoxin, a label, aligand, or a drug or liposome, etc.). Means of chemically conjugatingmolecules are well known to those of skill.

The procedure for attaching an effector to an antibody will varyaccording to the chemical structure of the effector and/or antibody.Polypeptides typically contain variety of functional groups; e.g.,carboxylic acid (COOH) or free amine (—NH₂) groups, that are availablefor reaction with a suitable functional group on an effector molecule tobind the effector thereto.

Alternatively, the antibody and/or the effector can be derivatized toexpose or attach additional reactive functional groups. Thederivatization can involve attachment of any of a number of linkermolecules such as those available from Pierce Chemical Company, RockfordIllinois.

A “linker”, as used herein, is a molecule that is used to join thetargeting molecule to the effector molecule. The linker is capable offorming covalent bonds to both the targeting molecule and to theeffector molecule. Suitable linkers are well known to those of skill inthe art and include, but are not limited to, straight or branched-chaincarbon linkers, heterocyclic carbon linkers, or peptide linkers. Wherethe targeting molecule and the effector molecule are polypeptides, thelinkers may be joined to the constituent amino acids through their sidegroups (e.g., through a disulfide linkage to cysteine). However, in apreferred embodiment, the linkers will be joined to the alpha carbonamino or carboxyl groups of the terminal amino acids.

A bifunctional linker having one functional group reactive with a groupon a particular agent, and another group reactive with an antibody, maybe used to form the desired immunoconjugate. In certain embodiments,derivatization can involve chemical treatment of the targeting molecule,e.g., glycol cleavage of the sugar moiety of a the glycoprotein antibodywith periodate to generate free aldehyde groups. The free aldehydegroups on the antibody may be reacted with free amine or hydrazinegroups on an agent to bind the agent thereto. (See U.S. Pat. No.4,671,958). Procedures for generation of free sulfhydryl groups onpolypeptide, such as antibodies or antibody fragments, are also known(See U.S. Pat. No. 4,659,839).

Many procedures and linker molecules for attachment of various compoundsincluding radionuclide metal chelates, toxins and drugs to proteins suchas antibodies are known (see, e.g., European Patent Application No.188,256; U.S. Pat. Nos. 4,671,958, 4,659,839, 4,414,148, 4,699,784;4,680,338; 4,569,789; and 4,589,071; and Borlinghaus et al. (1987)Cancer Res. 47: 4071-4075). In particular, production of variousimmunotoxins is well-known within the art and can be found, for examplein “Monoclonal Antibody-Toxin Conjugates: Aiming the Magic Bullet,”Thorpe et al., Monoclonal Antibodies in Clinical Medicine, AcademicPress, pp. 168-190 (1982), Waldmann (1991) Science, 252: 1657, U.S. Pat.Nos. 4,545,985 and 4,894,443.

In some circumstances, it is desirable to free the effector from thetargeting molecule when the chimeric molecule has reached its targetsite. Therefore, chimeric conjugates comprising linkages which arecleavable in the vicinity of the target site may be used when theeffector is to be released at the target site. Cleaving of the linkageto release the agent from the antibody may be prompted by enzymaticactivity or conditions to which the immunoconjugate is subjected eitherinside the target cell or in the vicinity of the target site. When thetarget site is a tumor, a linker which is cleavable under conditionspresent at the tumor site (e.g. when exposed to tumor-associated enzymesor acidic pH) may be used.

A number of different cleavable linkers are known to those of skill inthe art. See U.S. Pat. Nos. 4,618,492; 4,542,225, and 4,625,014. Themechanisms for release of an agent from these linker groups include, forexample, irradiation of a photolabile bond and acid-catalyzedhydrolysis. U.S. Pat. No. 4,671,958, for example, includes a descriptionof immunoconjugates comprising linkers which are cleaved at the targetsite in vivo by the proteolytic enzymes of the patient's complementsystem. In view of the large number of methods that have been reportedfor attaching a variety of radiodiagnostic compounds, radiotherapeuticcompounds, drugs, toxins, and other agents to antibodies one skilled inthe art will be able to determine a suitable method for attaching agiven agent to an antibody or other polypeptide.

2 Conjugation of Chelates.

In certain preferred embodiments, the effector comprises a chelate thatis attached to an antibody or to an epitope tag. The prostate cancerspecific antibody bears a corresponding epitope tag or antibody so thatsimple contacting of the antibody to the chelate results in attachmentof the antibody with the effector. The combining step can be performedbefore the moiety is used (targeting strategy) or the target tissue canbe bound to the antibody before the chelate is delivered. Methods ofproducing chelates suitable for coupling to various targeting moietiesare well known to those of skill in the art (see, e.g., U.S. Pat. Nos.6,190,923, 6,187,285, 6,183,721, 6,177,562, 6,159,445, 6,153,775,6,149,890, 6,143,276, 6,143,274, 6,139,819, 6,132,764, 6,123,923,6,123,921, 6,120,768, 6,120,751, 6,117,412, 6,106,866, 6,096,290,6,093,382, 6,090,800, 6,090,408, 6,088,613, 6,077,499, 6,075,010,6,071,494, 6,071,490, 6,060,040, 6,056,939, 6,051,207, 6,048,979,6,045,821, 6,045,775, 6,030,840, 6,028,066, 6,022,966, 6,022,523,6,022,522, 6,017,522, 6,015,897, 6,010,682, 6,010,681, 6,004,533, and6,001,329).

3) Production of Fusion Proteins.

Where the antibody and/or the effector is relatively short (i.e., lessthan about 50 amino acids) they can be synthesized using standardchemical peptide synthesis techniques. Where both molecules arerelatively short the chimeric molecule may be synthesized as a singlecontiguous polypeptide. Alternatively the targeting molecule and theeffector molecule may be synthesized separately and then fused bycondensation of the amino terminus of one molecule with the carboxylterminus of the other molecule thereby forming a peptide bond.Alternatively, the targeting and effector molecules can each becondensed with one end of a peptide spacer molecule thereby forming acontiguous fusion protein.

Solid phase synthesis in which the C-terminal amino acid of the sequenceis attached to an insoluble support followed by sequential addition ofthe remaining amino acids in the sequence is the preferred method forthe chemical synthesis of the polypeptides of this invention. Techniquesfor solid phase synthesis are described by Barany and Merrifield,Solid-Phase Peptide Synthesis; pp. 3-284 in The Peptides: Analysis,Synthesis, Biology. Vol. 2: Special Methods in Peptide Synthesis, PartA., Merrifield, et al. J. Am. Chem. Soc., 85: 2149-2156 (1963), andStewart et al., Solid Phase Peptide Synthesis, 2nd ed. Pierce Chem. Co.,Rockford, Ill. (1984).

In certain embodiments, the chimeric fusion proteins of the presentinvention are synthesized using recombinant DNA methodology. Generallythis involves creating a DNA sequence that encodes the fusion protein,placing the DNA in an expression cassette under the control of aparticular promoter, expressing the protein in a host, isolating theexpressed protein and, if required, renaturing the protein.

DNA encoding the fusion proteins of this invention can be prepared byany suitable method, including, for example, cloning and restriction ofappropriate sequences or direct chemical synthesis by methods such asthe phosphotriester method of Narang et al. (1979) Meth. Enzymol. 68:90-99; the phosphodiester method of Brown et al. (1979)Meth. Enzymol.68: 109-151; the diethylphosphoramidite method of Beaucage et al. (1981)Tetra. Lett., 22: 1859-1862; and the solid support method of U.S. Pat.No. 4,458,066.

Chemical synthesis produces a single stranded oligonucleotide. This canbe converted into double stranded DNA by hybridization with acomplementary sequence, or by polymerization with a DNA polymerase usingthe single strand as a template. One of skill would recognize that whilechemical synthesis of DNA is limited to sequences of about 100 bases,longer sequences can be obtained by the ligation of shorter sequences.

Alternatively, subsequences can be cloned and the appropriatesubsequences cleaved using appropriate restriction enzymes. Thefragments can then be ligated to produce the desired DNA sequence.

In certain embodiments DNA encoding fusion proteins of the presentinvention can be cloned using PCR cloning methods.

While the antibody and the effector are, in certain embodiments,essentially joined directly together, one of skill will appreciate thatthe molecules can be separated by a spacer, e.g., a peptide spacerconsisting of one or more amino acids (e.g., (Gly₄Ser)₃ (SEQ ID NO:1).Generally the spacer will have no specific biological activity otherthan to join the proteins or to preserve some minimum distance or otherspatial relationship between them. However, the constituent amino acidsof the spacer may be selected to influence some property of the moleculesuch as the folding, net charge, or hydrophobicity.

The nucleic acid sequences encoding the fusion proteins can be expressedin a variety of host cells, including E. coli, other bacterial hosts,yeast, and various higher eukaryotic cells such as the COS, CHO and HeLacells lines and myeloma cell lines. The recombinant protein gene will beoperably linked to appropriate expression control sequences for eachhost.

The plasmids of the invention can be transferred into the chosen hostcell by well-known methods such as calcium chloride transformation forE. coli and calcium phosphate treatment or electroporation for mammaliancells. Cells transformed by the plasmids can be selected by resistanceto antibiotics conferred by genes contained on the plasmids, such as theamp, gpt, neo and hyg genes.

Once expressed, the recombinant fusion proteins can be purifiedaccording to standard procedures of the art, including ammonium sulfateprecipitation, affinity columns, column chromatography, gelelectrophoresis and the like (see, generally, R. Scopes (1982) ProteinPurification, Springer-Verlag, N.Y.; Deutscher (1990) Methods inEnzymology Vol. 182: Guide to Protein Purification., Academic Press,Inc. N.Y.). Substantially pure compositions of at least about 90 to 95%homogeneity are preferred, and 98 to 99% or more homogeneity are mostpreferred for pharmaceutical uses. Once purified, partially or tohomogeneity as desired, the polypeptides may then be usedtherapeutically.

One of skill in the art would recognize that after chemical synthesis,biological expression, or purification, the fusion protein may possess aconformation substantially different than the native conformations ofthe constituent polypeptides. In this case, it may be necessary todenature and reduce the polypeptide and then to cause the polypeptide tore-fold into the preferred conformation. Methods of reducing anddenaturing proteins and inducing re-folding are well known to those ofskill in the art (see, e.g., Debinski et al. (1993) J. Biol. Chem., 268:14065-14070; Kreitman and Pastan (1993) Bioconjug. Chem., 4: 581-585;and Buchner, et al. (1992) Anal. Biochem., 205: 263-270).

One of skill would recognize that modifications can be made to thefusion proteins without diminishing their biological activity. Somemodifications may be made to facilitate the cloning, expression, orincorporation of the targeting molecule into a fusion protein. Suchmodifications are well known to those of skill in the art and include,for example, a methionine added at the amino terminus to provide aninitiation site, or additional amino acids placed on either terminus tocreate conveniently located restriction sites or termination codons.

IV) Pharmaceutical Compositions.

The prostate cancer specific antibodies, and/or chelates, and/orchimeric moieties of this invention are useful for parenteral, topical,oral, or local administration (e.g. injected into a tumor site), aerosoladministration, or transdermal administration, for prophylactic, butprincipally for therapeutic treatment. The pharmaceutical compositionscan be administered in a variety of unit dosage forms depending upon themethod of administration. For example, unit dosage forms suitable fororal administration include powder, tablets, pills, capsules andlozenges. It is recognized that the fusion proteins and pharmaceuticalcompositions of this invention, when administered orally, are preferablyprotected from digestion. This can be accomplished by a number of meansknown to those of skill in the art, e.g., by complexing the protein witha composition to render it resistant to acidic and enzymatic hydrolysisor by packaging the protein in an appropriately resistant carrier suchas a liposome. Means of protecting proteins from digestion are wellknown in the art.

The pharmaceutical compositions of this invention are particularlyuseful for parenteral administration, such as intravenous administrationor administration into a body cavity or lumen of an organ. Thecompositions for administration will commonly comprise a solution of thechimeric molecule dissolved in a pharmaceutically acceptable carrier,preferably an aqueous carrier. A variety of aqueous carriers can beused, e.g., buffered saline and the like. These solutions are sterileand generally free of undesirable matter. These compositions may besterilized by conventional, well known sterilization techniques. Thecompositions may contain pharmaceutically acceptable auxiliarysubstances as required to approximate physiological conditions such aspH adjusting and buffering agents, toxicity adjusting agents and thelike, for example, sodium acetate, sodium chloride, potassium chloride,calcium chloride, sodium lactate and the like. The concentration ofchimeric molecule in these formulations can vary widely, and will beselected primarily based on fluid volumes, viscosities, body weight andthe like in accordance with the particular mode of administrationselected and the patient's needs.

Thus, a typical pharmaceutical composition for intravenousadministration would be about 0.1 to 10 mg per patient per day. Dosagesfrom 0.1 up to about 100 mg per patient per day may be used,particularly when the drug is administered to a secluded site and notinto the blood stream, such as into a body cavity or into a lumen of anorgan. Actual methods for preparing parenterally administrablecompositions will be known or apparent to those skilled in the art andare described in more detail in such publications as Remington'sPharmaceutical Science, 15th ed., Mack Publishing Company, Easton,Pennsylvania (1980).

The compositions containing the present antibodies and/or chimericmolecules (e.g. fusion proteins) or a cocktail thereof (i.e., with otherproteins) can be administered for therapeutic treatments. In therapeuticapplications, compositions are administered to a patient suffering froma disease, e.g., a cancer, in an amount sufficient to cure or at leastpartially arrest the disease and its complications. An amount adequateto accomplish this is defined as a “therapeutically effective dose.”Amounts effective for this use will depend upon the severity of thedisease and the general state of the patient's health.

Single or multiple administrations of the compositions may beadministered depending on the dosage and frequency as required andtolerated by the patient. In any event, the composition should provide asufficient quantity of the proteins of this invention to effectivelytreat the patient.

It will be appreciated by one of skill in the art that there are someregions that are not heavily vascularized or that are protected by cellsjoined by tight junctions and/or active transport mechanisms whichreduce or prevent the entry of macromolecules present in the bloodstream

One of skill in the art will appreciate that in these instances, thetherapeutic compositions of this invention can be administered directlyto the tumor site. Thus, for example, prostate tumors can be treated byadministering the therapeutic composition directly to the tumor site(e.g., through a surgically implanted catheter).

Alternatively, the therapeutic composition can be placed at the targetsite in a slow release formulation. Such formulations can include, forexample, a biocompatible sponge or other inert or resorbable matrixmaterial impregnated with the therapeutic composition, slow dissolvingtime release capsules or microcapsules, and the like.

Typically the catheter or time release formulation will be placed at thetumor site as part of a surgical procedure. Thus, for example, wheremajor tumor mass is surgically removed, the perfusing catheter or timerelease formulation can be emplaced at the tumor site as an adjuncttherapy. Of course, surgical removal of the tumor mass may be undesired,not required, or impossible, in which case, the delivery of thetherapeutic compositions of this invention may comprise the primarytherapeutic modality.

V. Kits.

Where a radioactive, or other, effector is used as a diagnostic and/ortherapeutic agent, it is frequently impossible to put the ready-for-usecomposition at the disposal of the user, because of the often poor shelflife of the radiolabeled compound and/or the short half-life of theradionuclide used. In such cases the user can carry out the labelingreaction with the radionuclide in the clinical hospital, physician'soffice, or laboratory. For this purpose, or other purposes, the variousreaction ingredients can then be offered to the user in the form of aso-called “kit”. The kit is preferably designed so that themanipulations necessary to perform the desired reaction should be assimple as possible to enable the user to prepare from the kit thedesired composition by using the facilities that are at his disposal.Therefore the invention also relates to a kit for preparing acomposition according to this invention.

In certain embodiments, such a kit according to the present inventioncomprises one or more prostate cancer specific antibodies of thisinvention. The antibodies can be provided, if desired, with inertpharmaceutically acceptable carrier and/or formulating agents and/oradjuvants is/are added. In addition, the kit optionally includes asolution of a salt or chelate of a suitable radionuclide (or otheractive agent), and (iii) instructions for use with a prescription foradministering and/or reacting the ingredients present in the kit.

The kit to be supplied to the user may also comprise the ingredient(s)defined above, together with instructions for use, whereas the solutionof a salt or chelate of the radionuclide, defined sub (ii) above, whichsolution has a limited shelf life, may be put to the disposal of theuser separately.

The kit can optionally, additionally comprise a reducing agent and/or,if desired, a chelator, and/or instructions for use of the compositionand/or a prescription for reacting the ingredients of the kit to formthe desired product(s). If desired, the ingredients of the kit may becombined, provided they are compatible.

In certain embodiments, the complex-forming reaction with the prostatecancer specific antibody can simply be produced by combining thecomponents in a neutral medium and causing them to react. For thatpurpose the effector may be presented to the antibody in the form of achelate.

When kit constituent(s) are used as component(s) for pharmaceuticaladministration (e.g. as an injection liquid) they are preferablysterile. When the constituent(s) are provided in a dry state, the usershould preferably use a sterile physiological saline solution as asolvent. If desired, the constituent(s) may be stabilized in theconventional manner with suitable stabilizers, for example, ascorbicacid, gentisic acid or salts of these acids, or they may comprise otherauxiliary agents, for example, fillers, such as glucose, lactose,mannitol, and the like.

While the instructional materials, when present, typically comprisewritten or printed materials they are not limited to such. Any mediumcapable of storing such instructions and communicating them to an enduser is contemplated by this invention. Such media include, but are notlimited to electronic storage media (e.g., magnetic discs, tapes,cartridges, chips), optical media (e.g., CD ROM), and the like. Suchmedia may include addresses to internet sites that provide suchinstructional materials.

EXAMPLES

The following examples are offered to illustrate, but not to limit theclaimed invention.

Example 1 Identification of Clinically Significant Tumor Antigens bySelecting Phage Antibody Library on Tumor Cells in Situ Using LaserCapture Microdissection Experimental Procedures

Creating a Sublibrary Enriched for Binders to Functional Tumor CellSurface Epitopes

A sublibrary was created by selecting a naïve phage antibody displaylibrary on a panel of tumor cell lines under internalizing conditions.The preparation and selection of a phage antibody display library hasbeen described previously (Liu et al. (2004) Cancer Res. 64: 704-710;Poul et al. (2000) J Mol. Biol. 301: 1149-1161). Briefly the phagelibrary was preincubated with a panel of non-tumorigenic cells includingBPH-1, human mammary epithelial cells, MCF10A, and human fibroblasts toremove binders to common cell surface antigens. The predepleted librarywas then incubated with a panel of prostate cancer cell lines (PC3 andDu-145) at 37° C. for 2 h; washed twice with 100 mM glycine, pH 2.8, inthe presence of 150 mM NaCl; and washed once with PBS, pH 7.0.Internalized phage were recovered by lysing the cells with 100 mMtriethylamine, propagated in TG1, and purified by precipitation withpolyethylene glycol 8000 as described previously (1), thereby creating asublibrary that is enriched for binders to internalizing cell surfacemolecules. The sublibrary contained 1-5×10⁵ copies of about 10⁶independent clones at the concentration of 1-5×10¹¹ cfu/ml.

Selection of Antibodies Targeting Tumor Cells in Situ by LCM

Selections were performed on both frozen and paraffin-embedded prostatecancer tissues. For selection on frozen tissue slides, 5 μm sectionsfrom prostate cancer specimens were cut onto Leica MembraneSlides(MicroDissect, Mittenaar, Germany), stained with hematoxylin, andincubated with the sublibrary (0.5 ml of 5×10¹¹ cfu/ml stock) at roomtemperature for 1 h. The slides were then washed three times in PBS toremove unbound phage and prepared for LCM by dehydration in 70, 95, and100% ethanol in series. For selection on paraffin-embedded tissue, 5 μmsections were cut onto film-coated Leica slides, xylene-treated toremove paraffin, rehydrated through serial 100, 95, and 75% ethanol,placed in PBS with blocking solution at room temperature for 1 h,washed, and incubated with the sublibrary described above. LCM wasperformed using the Leica AS LMD (Leica Microsystems GmbH, Wetzlar,Germany) that uses a UV pulse laser to excise selected cells fromsurrounding tissues. Typically 20-50 tumor cells were procured at a timeby generating a closed laser path around the group of cells of interest.The cells were then dropped into collection tubes by electrostatic forceand gravity. These tissue pieces were stored at −80° C. until analysis.

Recovery of Phage Antibody from LCM-Procured Tissue Pieces

Genes encoding scFv fragments were amplified by PCR from LCM-procuredtumor pieces using the following primer pairs: Fd2 (TTT TTG GAG ATT TTCAAC, SEQ ID NO:348) and Fdseq (GAA TTT TCT GTA TGA GG, SEQ ID NO:349).The amplified fragments were digested by SfiI and NotI, purified, andligated into Fd-Tet vectors precut with the same restriction enzymes(Liu et al. (2004) Cancer Res. 64: 704-710). The ligation products wereused to transform chemically competent TG1. Each LCM library contained>10⁵ independent clones. The number of unique phage antibodies wasdetermined by patterns of BstNI digestion (Liu et al. (2004) Cancer Res.64: 704-710; Liu and Marks (2000) Anal. Biochem. 286: 119-128). Whenrestriction digestion patterns showed ambiguity, phage antibody geneswere sequenced to determine their uniqueness.

Initial Analysis of Selection Output by FACS

Prostate cancer (PC3 and Du-145) or non-tumorigenic control (BPH-1)cells were incubated with phage antibody (5×10¹¹ cfu/ml) for 1 h at 4°C. Bound phages were detected by FACS (LSRII, BD Biosciences) usingbiotinylated anti-M13 antibody (Sigma, diluted 1:1000) followed bystreptavidin-phycoerythrin (BIOSOURCE/Invitrogen, diluted 1:1000) (Liuet al. (2004) Cancer Res. 64: 704-710) (see, e.g., FIG. 3 ). Phageantibodies that showed positive binding were identified and sequenced.

Further Analysis of Selection Output by Immunohistochemistry

Sections of prostate cancer tissue (frozen and paraffin-embedded) andnormal human tissues were provided by the Genitourinary Tissue Core ofthe University of California, San Francisco Comprehensive Cancer Center.All tissues were collected with consent at the Core using protocolsapproved by the Committee on Human Research. For immunohistochemicalanalysis, tissue sections were incubated with biotinylated, monomericscFv (50 μg/ml) at room temperature for 1 h, washed with PBS, andincubated with horseradish peroxidase-conjugated streptavidin at adilution of 1:1000 (Sigma) for 30 min. Binding was detected usingdiaminobenzidine (DAB) as the substrate (Sigma) (Liu et al. (2004)Cancer Res. 64: 704-710) (see, e.g., FIG. 4).

Expression, Purification, and Biotinylation of scFv Fragments

Two forms of soluble antibody fragments, scFv and (scFv′)₂, wereproduced (Liu et al. (2004) Cancer Res. 64: 704-710). The scFv gene wassubcloned into the secretion vector pUC119mycHis, adding a c-Myc epitopetag and hexahistidine tag at the C terminus of the scFv (Id.). To createthe (scFv′)₂ dimer for immunoliposome studies, the c-Myc epitope tag wasremoved, and a free cysteine was introduced at the C terminus of thescFv preceding the hexahistidine tag as described previously (Liu et al.(2004) Cancer Res. 64: 704-710). scFv monomer or (scFv′)2 dimer proteinswere harvested from the bacterial periplasmic space and purified by IMACas described previously (Id.). To biotinylate scFv for FACS analysis,affinity-captured monomeric scFv fragments were washed in PBS andincubated with NHS-LC-biotin (Pierce) at 0.5 mg/ml for 20 min prior toelution with 250 mM imidazole.

Assay for Internalizing and Intracellular Delivery

Unilamellar liposomes composed of1,2-distearoyl-sn-glycero-3-phosphocholine, cholesterol, DiIC18(3)-DS,and β-(N-maleimido)propionyl poly(ethyleneglycol)-1,2-distearoyl-3-sn-phosphoethanolamine (molar ratio,6:6:0.03:0.03) were prepared as described previously (Nielsen et al.(2002) Biochim. Biophys. Acta 1591: 109-118; Saito et al. (2005) Exp.Neurol. 196: 381-389; Saito et al. (2004) Cancer Res. 64: 2572-2579).His₆-tagged (scFv′)₂ were reduced to the monomeric form throughincubation with 20 μg/ml 13-mercaptoethylamine for 45 min at roomtemperature (Nielsen et al. (2002) Biochim. Biophys. Acta 1591:109-118). The reduced monomeric scFv fragments were conjugated withDiICI 8(3)-DS liposomes in 30 μg of protein/μ mol of phospholipids at37° C. for 4 h. To assess intracellular liposome delivery,scFv′-conjugated liposomes were incubated at 37° C. for 2 h with cells,which were then washed three times with saline containing 1 mM EDTA, 250mM imidazole to remove cell surface-bound liposomes that failed tointernalize. Uptake of scFv-DiICI 8(3)-DS immunoliposomes was determinedby FACS and by an inverted fluorescence microscope (Eclipse TE300, NikonCorp.) (see, e.g., FIG. 5 ).

Results.

Selection of Phage Antibody Binding to Clinically Relevant InternalizingEpitopes by LCM

Selection was performed according to the scheme outlined in FIG. 1 . Weaimed to identify phage antibodies that bind to tumor epitopes presenton actual cases of cancer and to further identify a subset of functionalphage antibodies that bind to internalizing epitopes so that they may beexploited to deliver payload to the interior of tumor cells.

We devised a multistep strategy to achieve these aims (FIG. 1 ). First,a sublibrary was generated that is enriched for binders to cell surfacereceptors including those that are internalizing. This was accomplishedby counterselecting a naïve phage antibody library containing 5×10⁸unique scFv fragments on a panel of non-tumorigenic epithelial celllines to remove binders to common cell surface antigens followed byselecting on a panel of live tumor cell lines such as the hormonerefractory prostate cancer lines PC3 and Du-145 (Liu et al. (2004)Cancer Res. 64: 704-710; Liu and Marks (2000) Anal. Biochem. 286:119-128; O'Connell et al. (2002) J Mol. Biol. 321: 49-56; Huie, et al.(2001) Proc. Natl. Acad. Sci., USA, 98: 2682-2687). By manipulating theselection conditions to preferentially recover internalized phage, asublibrary enriched for internalizing phage antibody was created (Liu etal. (2004) Cancer Res. 64: 704-710; Gao et al. (2003) J. Immunol.Methods 274: 185-197; Poul et al. (2000) J. Mol. Biol. 301: 1149-1161;Becerril et al. (1999) Biochem. Biophys. Res. Commun. 255: 386-393).Next the enriched sublibrary was incubated with tumor tissue slides, andtumor cells along with bound phage were procured by LCM (FIG. 2 ). ThescFv genes were amplified by PCR and recloned into a phage displayvector to generate a population of phage antibody that were eitherscreened or used as input for the next round of selection (FIG. 2 ).Following one or two rounds of selection on tissue, the output wasscreened first on tumor cell lines to identify positive binders.Following sequencing, unique scFv fragments were further studied by IHCon tissue slides according to the scheme outlined in FIG. 1 . Thisselection scheme effectively restricts selection outcomes to phageantibodies that bind to epitopes present on both tumor cell lines andtumor cells in situ from actual cases. Moreover these antibodies possessinternalizing functions that can be exploited for targeted payloaddelivery. Antibodies that meet these criteria will likely havesignificant therapeutic values.

Initial Analysis of Selection Output: Binding to Tumor Cell Lines

Random clones from the sublibraries created after LCM-based selectionswere screened on PC3 and Du-145 cells by FACS (FIG. 3 ). More than 600clones from various LCM-derived sublibraries were screened. Only thoseclones that bound to both PC3 and Du-145 cells were chosen for furtheranalysis because they are more likely to recognize tumor cell surfaceantigens as opposed to artifacts associated with a particular tissueslide. The fraction of CaP cell line-binding clones ranged from 15 to88% (Table 4). Unique clones were identified by DNA sequencing. Thirteenunique phage antibodies were found from a total of 85 positive clonessequenced. We focused on two scFv fragments, UA20 and 585141, forfurther characterization. The UA20 scFv was obtained from selection onparaffin-embedded prostate cancer tissue. The 585II41 scFv was obtainedfrom selection on fresh frozen prostate cancer tissue.

TABLE 4 Summary of selection results. Four paraffin-embedded and twofrozen CaP tissues were used in the selection. The sublibrariesconstructed from PCR products contained 2-8 × 10⁵ unique clones. Bindersto both PC3 and Du-145 cell lines were identified from each sublibraryby FACS screening. Between 10 and 20 positive clones from each groupwere sequenced to identify unique clones. Thirteen unique clones wereidentified from a total of 85 clones sequenced. Tumor grades No. clonesin Cell line Cases Tissue slides (Gleason scores) sublibrary binders CaP1 Paraffin 3 + 4 5 × 10⁵  29/188 (15%) CaP 2 Paraffin 4 + 5 8 × 10⁵140/188 (75%) CaP 3 Paraffin 3 + 4 5 × 10⁵  72/288(25%) CaP 4 Paraffin3 + 4 2 × 10⁵  40/96 (42%) CaP 5 Frozen 4 + 5 7 × 10⁵  85/96(88%) CaP 6Frozen 3 + 4 5 × 10⁵  75/96(78%)

Further Analysis of Selection Output: Binding to Tumor Cells in Situ

Phage antibodies selected by LCM were expected to bind to clinicallyrelevant antigens on cancer cells in situ. We performedimmunohistochemical studies using soluble scFv fragments derived fromLCM-selected phage antibody on prostate cancer tissue sections. FIG. 4 ,panels A-C, shows the staining results of the UA20 and 585II41 scFvfragments on tissue specimens obtained from Gleason 3+4 patients. Onboth frozen and paraffin-embedded tissue slides, the UA20 scFv showed anintense staining of tumor epithelium with minimal staining of normaladjacent prostate epithelium (FIG. 4 , panels A and C). The 585II41 scFvalso stained tumor cells intensely on frozen tissue slides (FIG. 4 ,panel B). Some basal cells in normal epithelium adjacent to tumor werealso stained with reduced intensity (Table 5). The 585II41 scFv did notstain paraffin-embedded slides (data not shown), consistent with thefact that it was originally identified from selection on frozen tissueslides. These experiments indicate that antibodies obtained from LCMselection bind to antigens that exist in patient specimens and thus areclinically relevant to human prostate cancer. The corresponding antigensare likely targets for therapeutic intervention.

TABLE 5 Immunohistochemistry (IHC) results of the 585II41 and UA20 scFvfragments on a panel of frozen CaP and normal tissues. The numbers ofcases studied are indicated. Biotinylated scFv fragments were firsttested on cell lines to ensure binding activity and then used for IHCstudies. As a control, a random scFv with no binding activity to celllines was used to register the background level of staining. No change,no changei n staining level was observed when compared with the resultof the control scFv Tissues 585II41 UA20 CaP Strong stain on tumor(8/8); some Strong stain on stain on basal cells (5/8); and tumor (8/8);weak stain on adjacent normal some weak stain on (3/8) adjacent normal(2/8) Normal: Brain No change (7/7) No Change (4/4) Heart No change(1/1) No Change (4/4) Liver No change (3/4); Some bile duct No Change(4/4) stain (1/4) Kidney No change (4/4) No Change (4/4) Lung No changeof alveoli (5/5); stain No change of alveoli bronchial epithelial (5/5)and bronchial epithelial (5/5) Colon No change (4/4) No change (4/4)Bladder No change (2/3); faint epithelial No change (2/3); faint stain(1/3) epithelial and smooth muscle stain (1/3) Oral No change (3/4);some stain of No change (4/4) salivary gland (1/4)

In a subsequent study, additional immunohistochemistry was performed forthe UA20, 585II41, 585II56 and UA8 scFv fragments on a panel of frozenCaP and normal tissues (see, e.g., Table 6.). As a control, a scFv withno binding activity to cell lines was used to register the level ofbackground staining.

TABLE 6 Immunohistochemistry (IHC) results of the UA20, 585II41, 585II56and UA8 scFv fragments on a panel of frozen CaP and normal tissues. Thenumbers of cases studied are indicated. The 585II41 scFv binds to CD166,a known marker for prostate cancer. Tissues UA20 585II41 (H3 variant)585II56 UA8 CaP Strong stain on Strong stain on Strong stain on Strongstain on tumor (16/16); tumor (16/16); high grade tumor (16/16); someweak stain some stain on tumor (7/8); some stain on on adjacent basalcells variable stain on adjacent normal normal (3/16) (10/16); and lowgrade (4/8) (9/16) weak stain on and adjacent adjacent normal (7/16)normal (7/16) Normal Brain No stain (4/4) No stain (7/7) No stain (7/7)No stain (7/7) Heart No stain (4/4) No stain (1/1) No stain (1/1) Nostain (1/1) Liver No stain (4/4) No stain (3/4); No stain (4/4) No stain(4/4) some bile duct stain (1/4) Kidney No stain (4/4) No stain (4/4) Nostain (4/4) No stain (4/4) Lung No stain (5/5) No stain of No stain(5/5) No stain (5/5) alveoli (5/5); stain bronchial epithelial (5/5)Colon No stain (4/4) No stain except No stain (4/4) No stain (4/4)ganglion (4/4) Bladder No stain (2/3); No stain (2/3); No stain (3/3) Nostain (2/3); faint stain (1/3) faint epithelial stain faint smooth (1/3)muscle stain (1/3) Oral No stain (4/4) No stain (3/4); No stain (4/4) Nostain (4/4) some stain of salivary gland (1/4)

Tissue Specificity

To study the cross-reactivity of scFv fragments with normal tissues, weperformed IHC studies on a panel of normal frozen human tissues usingpurified 585II41 and UA20 scFv fragments (Table 5). Compared withcontrols, the 585II41 scFv showed no significant staining on most normaltissues studied, including the brain, kidney, and heart. There was,however, significant staining of bronchial epithelial cells and skineccrines. The UA20 scFv, on the other hand, showed a more restrictedstaining pattern. At the concentration tested (50 μg/ml), the UA20 scFvshowed strong staining on prostate cancer tissues but no significantstaining on the panel of normal tissues studied (Table 5). We concludethat both scFv fragments recognize tumor cells in situ, and the UA20scFv has very low cross-reactivity to normal human tissues.

Internalization and Payload Delivery to Prostate Cancer Cells

Phage antibodies selected by LCM were derived from a phage populationthat was panned on tumor cell lines using a functional selection processtargeting receptor-mediated endocytosis. To confirm that selected phageantibodies possessed this phenotype and were endocytosed by CaP cells,the UA20 scFv′ with a free cysteine at the C terminus was produced andconjugated to maleimide-activated liposomes containing a fluorescentprobe, DiIC18(3)-DS, and incubated with BPH-1 (control), PC3, and Du-145cells. These immunoliposomes were efficiently endocytosed by both PC3and Du-1 45 cells (FIG. 5A-5C) with minimal uptake into BPH-1 cells (5).Without conjugated scFv fragments, untargeted liposomes were not takenup by prostate cancer cells (FIG. 5C). Like the UA20 scFv-ILs, the585II41-targeted liposomes were also efficiently taken up by prostatecancer cells (PC3 and Du-145) (data not shown). These experimentsdemonstrate that scFv antibodies selected by LCM retain internalizingfunctions and are capable of mediating efficient and specific payloaddelivery. These antibodies are candidates for the development oftargeted therapeutics against prostate cancer.

Identification of ALCAM as a Tumor Antigen

The 585II41 scFv was sequenced and found to be highly homologous to apreviously identified scFv, H3. These two scFv fragments differ by onlytwo amino acids, none of which are in the CDR3 region that is criticalfor antigen binding (data not shown). The antigen recognized by the H3scFv has been identified previously by us as ALCAM, also known as MEMDor CD166 (Kobata and Amano (2005) Immunol. Cell Biol. 83: 429-439). Wehypothesized that the 585II41 scFv is a variant of the H3 scFv and bindsto ALCAM. To test this hypothesis, we performed competition experimentsusing both H3 scFv and IgG to compete with the 585II41 scFv for bindingto prostate cancer cells (Du-145). As controls, an scFv and itscorresponding IgG that to ALCAM-expressing cells were included in theexperiment. FACS analysis showed that both H3 scFv and IgG competed awaybinding by 585II41 scFv, whereas the control scFv and IgG did not (FIG.6A). This indicates that the H3 scFv and the 585II41 scFv target thesame antigen, i.e. ALCAM.

To further confirm that 585II41 scFv binds to ALCAM, we used 585II41scFv to immunoprecipitate (IP) its target antigen from prostate cancercell lysates. We probed the IP product with a commercial monoclonalantibody raised against a unique ALCAM peptide (FIG. 6B). Thisanti-ALCAM mAb recognized the IP product of 585II41 scFv but not that ofthe control OA12 scFv, thus confirming that ALCAM is the antigentargeted by the 585II41 scFv. In agreement with our own IHC studies,ALCAM has been shown by others to be overexpressed in 86% of prostatecancer cases (Kristiansen et al. (2005) J. Pathoi. 205: 359-376). Thefact that we identified a binder to a validated prostate cancer markerindicates that our LCM-based selection method is indeed capable ofidentifying clinically relevant tumor antigens. The antigen recognizedby the UA20 scFv is being further characterized.

Discussion

The success of targeted cancer therapy depends in part on theavailability of a panel of targeting agents such as mAbs that recognizetumor cell surface antigens present in clinical specimens. Much work hasbeen done to generate mAbs against cell lines derived from primarytumor. It has become evident, however, that when removed from theiroriginal tissue environment cultured tumor cells variably up- anddown-regulate expression of cell surface molecules relative to primarytumor cells. It is challenging yet desirable to identify the overlappingsurface epitope space between tumor cell lines and tumor cells in actualcases.

We developed an LCM-based strategy that allows the selection of phageantibody against tumor cells in situ within their proper stromalmicroenvironment. By preselecting a naïve phage antibody library on apanel of tumor cell lines under internalizing conditions, we created asublibrary that is enriched for binders to functional cell surfaceepitopes. This sublibrary was then used for further selection on tissueslides. By precisely procuring tumor cells along with bound phage byLCM, we identified phage antibodies that bind to clinically representedtumor antigens. These antibodies meet the following criteria 1) bindingto internalizing cell surface epitopes present on tumor cell lines and2) binding to epitopes present on tumor cells in situ. The ability todeliver payload intracellularly to target cells present in actual casesof human cancer makes these antibodies attractive candidates fortherapeutic development.

We identified ALCAM, also known as MEMD or CD166, as the target for oneof the selected antibodies. ALCAM, a member of the immunoglobulinsuperfamily, was originally shown to be overexpressed on highlymetastatic melanoma cells (Oegen et al. (1998) Am. J. Pathol. 152:805-813). Recently it has been shown to be overexpressed in prostatecarcinomas and to be predictive of prostate-specific antigen relapse(Kristiansen et al. (2005) J. Pathol. 205: 359-376). The fact that wefound an scFv targeting a validated prostate cancer maker demonstratesthe effectiveness of our approach.

ALCAM has also been identified by selecting a phage antibody library onan ovarian tumor cell line, and an immuno-toxin has been made using theanti-ALCAM scFv (Piazza et al. (2005)J Cell Sci. 118: 1515-1525). Asthis study dealt with cell line selection only, future IHC study willhelp determine whether ALCAM is indeed a marker for ovarian cancer.Therapies targeting ALCAM should also take into consideration itsdistribution on normal tissues as our IHC study showed that ALCAM isexpressed on normal bronchial epithelial cells.

The sublibraries that were used for the LCM-based selection weregenerated from selection on tumor cell lines following counterselectionon a panel of non-tumorigenic cell lines. As no cell lines are trulynormal, it is possible that these non-tumorigenic cell lines share somesurface antigens with tumor cells. To account for this possibility andto preserve antigens that are overexpressed, if not exclusivelyexpressed, by tumor cells, we performed a moderate counterselection. Weaimed to reduce binders to the most common cell surface antigens but notto eliminate all binders that cross-react with non-tumorigenic celllines. The issues of tumor specificity and clinical relevance wereaddressed by direct selection and analysis on tissue sections instead.

We found some unexpected features associated with the LCM-basedselection that may have hindered the application of LCM in phageantibody display. Most curiously, phage bound to LCM-procured tissuepieces seemingly lose their ability to infect bacteria, posing achallenge to library selection. We had initially sought to recover boundphage by standard methods, i.e. elution of phage with high pH bufferfollowed by neutralization and infection of TG1 bacterial cells (Lu andKapila (2004) Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 98:692-697; Yao et al. (2005) Am. J. Pathol. 166, 625-636). However, littlebacterial growth was observed under various culture conditions (data notshown). This phenomenon was seen even in manually dissected tissuepieces that were not exposed to the UV laser used in the Leica LMDsystem (data not shown). Exposure to ethanol during slide preparationfor LCM seems to be a factor contributing to the observed reduction inphage viability. Regardless of the cause, we circumvented this problemby using the genomes of phages bound to the procured cancer cell piecesas templates for amplification of scFv genes by PCR.

We identified 13 unique phage antibodies after sequencing 85tumor-reactive clones. Because the sample size was small, it was notpossible to predict the total number of unique clones in the selectionoutput. Determining population diversity based on limited sample size isa complex statistical problem that cannot be solved by simpleextrapolation (Hughes et al. (2001) Appl. Environ. Microbiol. 67:4399-4406; Hughes and Hellmann (2005) Meth. Enzymol. 397: 292-308).

Although LCM has the capacity to procure a single cell, we generallyopted to procure a group of 20-50 tumor cells for phage antibodyselection. We found that it was rather difficult to recover phageantibodies from single cell procurement even by PCR amplification. Inthe rare cases that the phage antibodies were recovered, the diversityof scFv fragments was very low (in two of three cases, only a singleunique clone was found among the 20 sequenced). Either the UV laser pathencircling the single cell came too close to the bound phage, therebydamaging its DNA and reducing its viability for recovery, or there maybe less than one recoverable phage bound per cell on tissue slides. Inany event, we found that it was practical to procure 20-50 cells at atime for phage selection. When a large cluster of topologicallycontiguous tumor cells cannot be found, we generally procured severalsmall three-to five-cell clusters for analysis.

In the future, we envision the creation of a generic sublibrary thatcontains binders to a broad spectrum of cell surface antigens. This canbe done by selecting the naïve phage display library on a large panel ofexisting tumor cell lines such as NCI 60 (Covell et al. (2005) Proteins59: 403-433; Garraway and Sellers (2006) Cancer Res. 66: 2506-2508).This sublibrary can then be used as a universal input for LCM-basedselection on tissues. Given the amount of paraffin-embedded and frozentissues already archived, we anticipate the discovery of increasingnumbers of functional epitopes present in actual cases of cancer.

Example 2 SPECT/CT and Biodistribution Study of UA20 scFv

To determine the efficiency of the UA20 scFv in tumor targeting in vivo,we performed molecular imaging studies with technetium(^(99m)Tc)-labeled scFv and a combined modality SPECT/CT, which allowssimultaneous tomographic imaging of gamma-emitting radiopharmaceuticalsand anatomic imaging with CT. Immunodeficient mice were injected with 1million Du-145 cells subcutaneously. Six days later when the tumor waspalpable, the mice were injected with either ^(99m)Tc-labeled UA20 scFvor a ^(99m)Tc-labeled control scFv (N3M2) and imaged with SPECT/CT, andimaged 3 h post injection. As shown in FIG. 9 , prostate cancerxenograft was recognized by ^(99m)Tc-labeled UA20 scFv but not thecontrol scFv, demonstrating the targeting specificity in vivo. The otherorgans that showed the greatest contrast were the kidneys, consistentwith the route of scFv excretion from the body.

Next, we performed biodistribution studies using the ^(99m)Tc-labeledUA20 and the control scFvs. Antibody accumulation in tumor, blood, andmajor organs was determined at 6 h post injection. As shown in FIGS. 10Aand 10B, the UA20 scFv showed about 17-fold higher tumor accumulation inmice carrying Du-145 xenografts than control mice.

Results of a subsequent biodistribution study are shown in Table 7.

TABLE 7 Biodistribution study. The values of % ID/g tissue for both theUA20 scFv and the control non-binding N3M2 scFv were shown. Theexperiment was done using ^(99m)Tc-labeled scFvs on Du-145 xenografts.Sm. Int., small intestine. Lg. Int., large intestine. Organ UA20 ScFvCtr scFv Liver 2.74 13.77 Heart 0.13 0.64 Kidney 81.44 81.47 Lung 0.571.38 Spleen 0.84 6.68 Pancreas 0.23 0.67 Stomach 0.64 0.56 Sm Int. 0.801.15 Lg. Int. 0.81 1.03 Muscle 0.06 0.35 Fat 0.07 0.23 Blood 0.37 1.97Tumor 4.40 0.26

It is noted that the UA20 scFv has unusually good biodistributionpatterns with tumor % ID/gm over 4. Most scFvs, without furthermodifications such as diabodies and minibodies, have % ID/gm about 1.Moreover, background in mouse is very low (several fold lower than otherscFvs that we have tested for all vital organs). Therefore, UA20 is anexcellent candidate for imaging and/or therapy.

Example 3 Additional Comments Regarding Antibodies

The H3 sequence is almost identical to clone #11 (not 10; differing byone a.a.). H3 is closely related to 585II41.1. K_(D) data for H3 isshown in FIG. 11 (KD=4.4 pM). To further clarify, 585II41 antibody bindsto ALCAM, and is a variant of 585II41.1 that is an H3 variant. 585II41and 585II41.1 have identical properties despite a one amino aciddifference.

The Examples provided above are correct as 585II41 (clone #10) binds toALCAM. It just that it is not exactly H3, which is 585II41.1 (clone#11).

It is understood that the examples and embodiments described herein arefor illustrative purposes only and that various modifications or changesin light thereof will be suggested to persons skilled in the art and areto be included within the spirit and purview of this application andscope of the appended claims. All publications, patents, and patentapplications cited herein are hereby incorporated by reference in theirentirety for all purposes.

1.-61. (canceled)
 62. An isolated antibody or antigen binding fragmentthereof that specifically binds a prostate cancer cell comprising aheavy chain variable region (HCVR) CDR1 (SEQ ID NO: 62), HCVR CDR2 (SEQID NO: 64), HCVR CDR3 (SEQ ID NO: 66), a light chain variable region(LCVR) CDR1 (SEQ ID NO: 223), LCVR CDR2 (SEQ ID NO: 225), and LCVR CDR3(SEQ ID NO: 227).
 63. The isolated antibody or antigen binding fragmentthereof of claim 62, wherein said antibody or antigen binding fragmentthereof comprises the variable heavy chain domain and the variable lightchain domain of the antibody UA20 (SEQ ID NO: 8).
 64. The isolatedantibody or antigen binding fragment thereof of claim 62, wherein saidantigen binding fragment is selected from the group consisting of a Fab,a (Fab′)2, an scFv, and an (ScFv′)2.
 65. The isolated antibody orantigen binding fragment thereof of claim 62, wherein said antigenbinding fragment is a single chain antibody UA20 (SEQ ID NO: 8).
 66. Theisolated antibody or antigen binding fragment thereof of claim 62further comprising an effector attached to the isolated antibody orantigen binding fragment.
 67. The isolated antibody or antigen bindingfragment thereof of claim 66, wherein said effector is selected from thegroup consisting of an epitope tag, a second antibody, a label, acytotoxin, a liposome, a radionuclide, a drug, a prodrug, a viralparticle, a cytokine, and a chelate.
 68. A pharmaceutical formulation,said formulation comprising a pharmaceutically acceptable excipient andan antibody or antigen binding fragment thereof according to claim 62.69. A pharmaceutical formulation, said formulation comprising apharmaceutically acceptable excipient and a chimeric moiety comprisingan effector attached to an antibody or antigen binding fragment thereofaccording to claim
 62. 70. The pharmaceutical formulation of claim 69,wherein said effector is selected from the group consisting of anepitope tag, a second antibody, a label, a cytotoxin, a liposome, aradionuclide, a drug, a prodrug, a viral particle, a cytokine, and achelate.
 71. A method of treating prostate cancer in a patient in needthereof comprising administering to the patient a chimeric moietycomprising an antibody attached to an anti-cancer drug or aradionuclide, wherein said antibody comprises a heavy chain variableregion (HCVR) CDR1 (SEQ ID NO: 62), HCVR CDR2 (SEQ ID NO: 64), HCVR CDR3(SEQ ID NO: 66), a light chain variable region (LCVR) CDR1 (SEQ ID NO:223), LCVR CDR2 (SEQ ID NO: 225), and LCVR CDR3 (SEQ ID NO: 227), andwherein the prostate cancer is treated.
 72. The method of claim 71,wherein said prostate cancer is a metastatic cancer.
 73. The method ofclaim 71, wherein said antibody comprises the variable heavy chaindomain and the variable light chain domain of the antibody UA20 (SEQ IDNO: 8).
 74. The method of claim 71, wherein said antibody is a singlechain antibody.
 75. The method of claim 74, wherein the variable lightchain domain is attached to the variable heavy chain domain by a(Gly₄Ser)3 (SEQ ID NO:1) linker.
 76. The method of claim 71, whereinsaid antibody is an antibody selected from the group consisting of aFab, a (Fab′)2, an scFv, and an (ScFv′)2.
 77. The method of claim 76,wherein said antibody is an scFv.
 78. The method of claim 71, whereinsaid chimeric moiety is internalized into a prostate cancer cell. 79.The method of claim 71, wherein said prostate cancer is a refractoryprostate cancer.
 80. The method of claim 71, wherein said chimericmoiety is formulated with a pharmaceutically acceptable excipient. 81.The method of claim 71, wherein said antibody is an intact antibody. 82.The method of claim 71, wherein said antibody is an IgG.